Volume 101 Number 5
D a v i d W. S m i t h
Publications of David W. Smith Smith DW, Blizzard RM, Wilkins L: The mental prognosis in hypothyroidism in infancy and childhood: A review of 128 cases, Pediatrics 19:1011, 1957. Smith DW, Blizzard RM, Wilkins L, Harrison HB: Idiopathic hypercalcemia: A case report with assays of Vitamin D in the serum, Pediatrics 24:258, 1959. Patau K, Smith DW, Therman E, Inhorn SL, Wagner HP: Multiple congenital anomaly caused by an extra autosome, Lancet 1:790, 1960. Smith DW, Patau K, Therman E, Inhorn SL: A new autosomal trisomy syndrome: Two cases of multiple congenital anomaly caused by an extra chromosome, J PEDIATR 57:338, 1960. Patau K, Therman E, Smith DW, DeMars R: Trisomy for chromosome No. 18 in man, Chromosoma 12:280, 1961. Therman E, Patau K, Smith DW, DeMars R: The D trisomy syndrome and XO gonadal dysgenesis in two sisters, Am J Hum Genet 13:193, 1961. Patau K, Therman E, Smith DW, Inhorn SL: Two cases of Da trisomy in man, Hereditas 47:239, 1961. Patau K, Therman E, Smith DW, Inhorn SL, Picken BF: Partial trisomy syndromes. I. Sturge-Weber disease, Am J Hum Genet 13:287, 1961. Patau K, Therman E, Smith DW, Ruess AL: Partial trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter, Cbromosoma 12:573, 1961. Smith DW, Patau K, Therman E: Autosomal trisomy syndromes, Lancet 2:211, 1961. Smith DW, Patau K, Therman E, Inhorn SL: The No. 18 trisomy syndrome, J PEDIATR 60:513, 1962. Leissring JC, Anderson JW, Smith DW: Uptake of antibodies by the intestine of the newborn infant, Am J Dis Child 103:160, 1962. Smith DW, Marden P, McDonald M J, Speckhard M: Lower incidence of sex chromatin in buccal smears of newborn females, Pediatrics 30:707, 1962. Copps SG, Gerritsen T, Smith DW, Waisman HA: Urinary excretion of 3,4-dihydroxyphenylafinine (DOPA) in two children of short stature with malnutrition, J PEDIATR 62:208, 1963. Smith DW, Patau K, lnhorn SL, Therman E: The D1 trisomy syndrome, J PEDIATR 62:326, 1963. Uchida IA, Patau K, Smith DW: Dermal patterns of 18 and Da trisomics, Am J Hum Genet 14:345, 1962. Smith DW: The No. 18 trisomy and D~ trisomy syndromes, Pediatr Clin North Am 10:389, 1963. Wegmann TG, Smith DW: Incidence of Klinefelter's syndrome among juvenile delinquents and felons, Lancet 1:274, 1963. Lemli L, Smith DW: The XO syndrome: A study of the differentiated phenotype in 25 patients, J PEDIATR 63:577, 1963. Ptacek L, Opitz JM, Smith DW, Gerritsen T, Waisman HA: The Cornelia DcLange syndrome, J PED~ATR63:1000, 1963. Kushner RS, Lemli L, Smith DW; Zinc glucagon in the management of idiopathic hypoglycemia, J PED1ATR 63:111 I, 1963.
Therman E, Patau K, DcMars R, Smith DW, Inhorn SL: lso/telo D~ mosaicism in a child with an incomplete D~ trisomy syndrome, Portugal Acta Biol 6:211, 1964. Smith DW, Lemlil L, Opitz JM: A newly recognized syndrome of multiple congenital anomalies, J PEDIATR 64:210, I964. Marden PM, Smith DW, McDonald M J: Congenital anomalies in the newborn, including minor variations: A study of 4412 babies by surface examination and buccal smear for sex chromatin, J PEDIATR 64:357, 1964. Nora J, Smith DW, Cameron JR: The route of insulin administration in the management of diabetes mellitus, J PEDIATR 64:547, 1964. Smith DW: Autosomal abnormalities, Am J Obstet Gynecol 90:1055, 1964. Smith DW, Bostian EK: Congenital anomalies associated with idiopathic mental retardation: Frequency in contrast to frequency in controls, in children with cleft lip and palate, and in those With ventricular septal defect, J PEDIATR 65:189, 1964. Wegmann T, Smith DW: Lower incidence of sex chromatin in newborn females delivered by Cesarean section, Pediatrics 34:419, 1964. Lemli L, Aron M, Smith DW: The action of Depo-Provera in three girls with idiopathic isosexuat precocity, 3 P~DIATR 65:888, 1964. Smith DW: Autosomal abnormalities in pediatrics, Pediatria 7:175, 1964. Rosenbloom AL, Smith DW: The natural history of metaphyseal dysostosis, J PEDIATR 66:857, 1965. Rosenbloom AL, Smith DW: Idiopathic anterior hypopituitarism in one of identical twins, J PEDIATR 67:34, 1965. Smith DW, Opitz JM, Inhorn SL: A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in two siblings, J PEDIATR 67:617, 1965. Tondury G, Smith DW: Fetal rubella pathology, J PEDIATR 68:867, 1966. Schmid W, Smith DW, Theiler K: Chromatinmuster in verschiedenen Zelltypen und Lokalisation yon Heterchromatin auf Metaphasechromosomen bei Mierotus agrestis, Mesocricetus auratus, Cavia porcellus und beim Menschen, Arch Klas-Stiff Vererb- Forsch, 1966, Rosenbloom AL, Smith DW, Cohan RC: Zinc glucagon in idiopathic hypoglycemia of infancy: Efficacy of long term control, Am J Dis Child 112:107, 1966. Rosenbloom AL, Smith DW: Varying expression for salt losing in related patients with congenital adrenal hyperptasia, Pediatrics 38:215, i966. Smith DW, Theiler K, Schachenmann G: Rib-gap defect with micrognathia, malformed tracheal cartilages, and redundant skin: A new pattern of defective development, J PEDIATR 69:799, 1966. Smith DW: Dysmorphology (Teratology), J PEDIATR 69:1150, 1966.
David W. Smith
Smith DW: Compendium on shortness of stature, J PEDIATR 70:463, 1967. Smith DW: Multiple malformation syndromes, J PED1ATR71:923, 1967. Frias JL, Smith DW: Diminished sweat pores in hypohidrotic ectodermal dysplasia: A new method for assessment, J PEDIATR 72:606, 1968~ Smith DW, Docter JM, Ferrier PE, Frias JL, Spock A: Possible localisation of the gene for cystic fibrosis of the pancreas to short arm of chromosome 5, Lancet 2:309, 1968. Aase JM, Smith DW: Dysmorphogenesis of joints, brain and palate: A new dominantly inherited syndrome, J PEDIATR 73:606, 1968. Laestadius ND, Aase JM, Smith DW: Normal inner canthal and outer orbital dimensions, J PEDIATR 74:465, 1969. Aase JM, Smith DW: Congenital anemia and triphalangeal thumbs: A new syndrome, J PEDIATR 74:471, 1969. Smith DW: Recognizable patterns of malformation in childhood, Birth Defects V, 2:255, 1969. Opitz JM, Johnson RC, McCreadie SR, Smith DW: The C syndrome of multiple congenital anomalies. Birth Defects 2:161, 1969. Mulvihill J J, Smith DW: Genesis of derrnatoglyphics, J PEDIATR 75:579, 1969. Smith DW, Aase JM: Polygenic inheritance of certain common malformations, J PEDIATR 76:653, 1970. Aase JM, Smith DW: Facial asymmetry and abnormalities of palms and ears: A dominantly inherited developmental syndrome, J PEDIATR 76:928, 1970. Marshall RE, Smith DW: Frontodigital syndrome: A dominantly inherited disorder with normal intelligence, J PEDIATR 77:129, 1970. Aase JM, Laestadius ND, Smith DW: Children of mothers who took LSD in pregnancy, Lancet 1:100, 1970. Popich GA, Smith DW: The genesis and significance of digital and palmar hand creases: Preliminary report, J PEDIATR 77:1017, 1970. Marshall RE, Graham CB, Scott CR, Smith DW: Syndrome of accelerated skeletal maturation and relative failure to thrive: A newly recognized clinical growth disorder, J PEDIATR 78:95, 1971. Latta R J, Graham CB, Aase J, Scham SM, and Smith DW: Larsen's syndrome: A skeletal dysplasia with multilple joint dislocations and unusual facies, J PEDIATR 78:291, 1971. Swanson S, Santen R, Smith DW: Multiple tentigines syndrome: New findings of hypogonadotrophism, hyposmia, and unilateral renal agenesis, J PED1ATR 78:1037, 1971. Gareis F J, Asper AC, Smith DW: Low X-chromatin frequency in untreated congenital adrenal hyperplasia, Lancet 1971. Gareis F J, Smith DW: Diminished stature-defective palate syndrome: A dominantly inherited disorder, J PED1ATR 79:470, 1971. Ruvalcaba RHA, Reichert A, Smith DW: A new familial syndrome with osseous dysplasia and mental deficiency, J PEDIATR 79:450, 1971. Gareis F J, smith DW, Summitt RL: The Russell-Silver syndrome without asymmetry, J PEDIATR 79:775, 1971. Guthrie RD, Aase J, Aspen"AC, Smith DW: The 4p-syndrome: A clinically recognizable chromosomal deletion syndrome, Am J Dis Child 122:421, 1971. Caldwell PD, Smith DW: The XXY (Klinefelter's) syndrome in childhood: Detection and treatment, J PEDIATR 80:250, t972.
The Journal of Pediatrics November 1982
Popich GA, Smith DW: Fontanels: Range of normal size, J PEDIATR 80:749, 1972. Smith DW, Popich G: Large fontanels in congenital hypothroidism: A potential clue toward earlier recognition, J PEDIATR 80:753, 1972. Bell DB, Smith DW: Myotonic dystrophy in the neonate, J PEDIATR 81:83, 1972. Hall BD, Smith DW: Prader-Willi syndrome, J PEDIATR 81:286, 1972. Furukawa CT, Hall BD, Smith DW: The Aarskog syndrome, J PEDIATR 81:1117, 1972. Patton RG, Christio DL, Smith DW, Beckwith JB: Cerebrohepato-renal syndrome of Zellweger, Am J Dis Child 124:840, 1972. Hall BD, Langer LO, Giedion A, Smith DW, Cohen MM, Beals RK, Brandner M Langer-Giedion syndrome, Birth Defects 1972. Quan L, Smith DW: The VATER association, J PED1ATR82:104, 1973. Aase JM, Wilson AC, Smith DW: Small ears in Down's syndrome: A helpful diagnostic aid, J PEDIATR 82:845, 1973. Weiswasser WH, Hal! BD, Delevan GW, Smith DW: Coffin-Siris syndrome: Two new cases, Am J Dis Child 125:838, 1973. Jones KL, Smith DW, Ulleland CN,' Streissguth AP: Pattern of malformation in offspring of chronic alcoholic mothers, Lancet 1:1267, 1973. Guthrie RD, Smith DW, Graham CB: Testosterone treatment for the micropenis during early childhood, J PEDIATR 83:247, 1973. Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ: A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies, J PEDIATR 83:280, 1973. Smith DW, Gong BT: Scalp hair patterning as a clue to earlY fetal brain development, J PEDIATR 83:374, 1973. Jones KL, Smith DW: Recognition of the fetal alcohol syndrome in early infancy, Lancet 2:999, 1973. Smith DW, Cohen MM Jr; Widow's peak scalp anomaly origin and relevance to ocular hypertelorism, Lancet 2:1127, 1973. Jones KL, Smith DW: Case report 3, Syndrome Identification 1:13, 1973. Jones KL, Guthrie RD, Smith DW: Case report 8, Syndrome Identification 1:10, 1973. Jones KL, Smith DW, Hall BD, Hall JG, Ebbin A J, Massoud H, Golbus MS: A pattern of craniofacial and limb defects secondary to aberrant tissue bands, J PEDIATR 84:90, 1974. Smith DW, Gong BT: Scalp-hair patterning: Its origin and significancerelative to early brain and upper facial development, Teratology 9:17, 1974. Weaver DD, Graham CB, Thomas IT, Smith DW: A new overgrowth syndrome in accelerated skeletal maturation, unusual facies, and camptodactyly, J PEDIATR 84:547, 1974. Greitzer L J, Jones KL, Schnall BS, Smith DW: Craniosynost0sisradial aplasia syndrome, J PED1ATR 84:723, 1974. Jones KL, Smith DW: Case report 21, Syndrome Identification 2:7, 1974. Wegmann J, Jones KL, Smith DW: Case report 13, Syndrome Identification 2:6, 1974. Thomas ITI Smith DW: Oligohydramnios, cause of the nonrenal features of Potter's syndrome, !ncluding pulmonary hypoplasia, J PEDIATR 84:811, 1974. Jones KL, Smith DW, Streissguth AP, Myrianthopoulos NC:
Volume 101 Number 5
Outcome in offspring of chronic alcoholic women, Lancet 1:1076, 1974. Weaver DD, Cohen MM Jr, Smith DW: The tricho-rhinophalangeal syndrome, J Med Genet 11:312, 1974. Schnall BS, Smith DW: Nonrandom laterality of malformations in paired structures, J PEDIATR 85:509, 1974. Karp LE, Smith DW, Omenn GS, Johnson SL, Jones KL: Use of ultrasound in the prenatal exclusion of primary microcephaty, Gynecol Invest 5:311, 1974. Smith DW: The VATER association, Am J Dis Child 128:767, 1974. Jones KL, Smith DW: Harvey MA, Hall BD, Quan L: Older paternal age and fresh gene mutation: Data on additional disorders, J PED1ATR 86:84, 1975. Feldman KW, Smith DW: Fetal phallic growth and penile standards for newborn males, J PEDIArR 86:395, 1975. Daentl DL, Smith DW, Scott CI, Hall BD, Gooding CA: Femoral hypoplasia-unusual facies syndrome, J PEDlaTR 86:107, 1975. Braun FHT, Jones KL, Smith DW: Breech presentation as an indicator of fetal abnormality, J PEDIATR 86:419, 1975. Jones KL, Smith DW: Tile Williams elfin facies syndromes: A new perspective, J PEDIATR 86:718, 1975. Hanson JW, Smith DW: U-shaped palatal defect in the Robin anomalad: Developmental and clinical relevance, J PEDIATR 87:30, 1975. Smith DW: Classification, nomenclature, and naming of morphologic defects, J PEDIATR 87:162, 1975. Jones KL, Smith DW: The fetal alcohol syndrome, Teratology 12:1, 1975. Hanson JW, Smith DW: The fetal hydantoin syndrome, J PEDIATr~ 87:285, 1975. Stephan M J, Hall BD, Smith DW, Cohen MM Jr: Macrocephaly in association with unusual cutaneous angiomatosis, J PEDIATR 87:353, 1975. Smith DW, Jones KL: Case report 28, Syndrome Identification 3:7, 1975. Smith DW, Jones KL: Testosterone in the early management of the ambiguous genitalia in the XY individual, Birth Defects 11:143, 1975. Smith DW, Simons FER: Rational diagnostic evaluation of the child with mental deficiency, Am J Dis Child 129:1285, 1975. Smith DW, Klein AM, Henderson JR, Myrianthopoulos NC: Congenital hypothyroidism: Signs and symptoms in the newborn period, J PEDIATR 87:953, 1975. Hanson JW, Jones KL, Smith DW: Fetal alcohol syndrome: Experience with 41 patients, JAMA 235:1458, 1976. Smith DW: Origin and relevance of aberrant scalp and upper facial hair patterning, Birth Defects 11:207, 1975. Hanson JW, Smith DW, Cohen MM Jr: Prominent lateral palatine ridges: Developmental and clinical relevance, J PZOIA"rR 89:54, 1976. Smith DW, Truog W. Rogers JE, Greitzer L J, Skinner AL, McCann J J, Harvey MAS: Shifting linear growth during infancy: Illustration of genetic factors in growth from fetal life through infancy, J PEDIATR 89:225, 1976. Smith DW: Prenatal growth deficiency, Birth Defects 12:31, 1976. Smith DW, Bartlett C, Harrah LM: Monozygotic twinning and the Duhamel anomalad (imperforate anus to sirenomelia): A non-random association between two aberrations in morphogenesis, Birth Defects 12:53, 1976.
D a v i d W. S m i t h
Hanson JW, Myrianthopoulos NC, Harvey MAS, Smith DW: Risks to the offspring of women treated with hydantoin anticonvulsants, with emphasis on the fetal hydantoin syndrome, J PEDtATR 89:662, 1976. Smith DW, Jones KL, Hanson JW: Perspectives on the cause and frequency of the fetal alcohol syndrome, Ann NY Acad Sci 273:138, 1976. Smith DW: Dysmorphology: Clinical patterns of human malformation, Univ Wash Med 3:11, 1976. Harvey MAS, Huntley RMC, Smith DW: Familial monozygotic twinning, J PEDIATR 90:246, 1977. Smith DW, Knudson RW: Aberrant scalp hair patterning in hypohidrotic ectodermal dysplasia, J PEDIATR 90:248, 1977. Smith DW: Micropenis and its management, Birth Defects 13:147, 1977. Smith DW: Clinical diagnosis and nature of chromosomal abnormalities, in Yunis J J, editor: New chromosomal syndromes, New York, 1977, Academic Press, Inc. Hanson JW, Sayers MP, Knopp LM, MacDonald C, Smith DW: Subtotal neonatal calvariectomy for severe craniosynostosis, J PEDIATR 91:257, 1977. Clarren SK, Smith DW: Prader-Willi syndrome, Am J Dis Child 131:798, 1977. Smith DW: Distal limb hypoplasia in the fetal hydantoin syndrome, Birth Defects 13:355, 1977. Smith DW: An appproach to clinical dysmorphology, J PEDIATR 91:690, 1977. Friedman JM, Hanson JW, Graham CB, Smith DW: SaethreChotzen syndrome: A broad and variable pattern of skeletal malformations, J PEDIATR 91:929, 1977. Smith DW: Teratogenicity of anticonvulsive medications, Am J Dis Child 131:1337, 1977. Clarren SK, Smith DW: Congenital deformities, Pediatr Clin North Am 24:665, 1977. Clarren SK, Alvord EC, Sumi SM, Streissguth AP, and Smith DW: Brain malformations related to prenatal exposure to ethanol, J PEDIATR 92:64, 1978. Streissguth AP, Herman CS, Smith DW: Intelligence, behavior, and dysmorphogenesis in the fetal alcohol syndrome: A report on 20 patients, J PEDIATR 92:363, 1978. Hanson JW, Streissguth AP, Smith DW: The effects of moderate alcohol consumption during pregnancy on fetal growth and morphogenesis, J PEDIATR 92:457, 1978. Miller P, Smith DW, Shepard TH: Maternal hyperthermia as a possible cause for anencephaly, Lancet 1:519, 1978. Smith DW, Takashima H: Protruding auricle: A neuromuscular sign, Lancet 1:747, 1978. Jones KL, Hanson JW, Smith DW: Palpebral fissure size in newborn infants, J PEDIATR 92:787, 1978. Chance PF, Smith DW: Hyperthemia and meningomyelocele and anencephaly, Lancet 1:769, 1978. Clarren SK, Smith DW: The fetal alcohol syndrome, N Engl J Med 293:1063, 1978. Smith DW, Greely M J: Unruly scalp hair in infancy: Its nature and relevance to problems of brain morphogenesis, Pediatrics 61:783, 1978. Streissguth AP, Herman CS, Smith DW: Stability of intelligence in the fetal alcohol syndrome: A preliminary report, Alcoholism (NY) 2:165, 1978. Smith DW, Clarren SK, Harvey MAS: Hyperthermia as a possible teratogenic agent, J PEDIATR 92:878, 1978.
David W. S m i t h
Smith DW, T6ndury G: Origin of the calvaria and its sutures, Am J Dis Child 132:662, 1978. Neidengard L, Carter TE, Smith DW: Klippel-Feil malformation complex in fetal alcohol syndrome, Am J Dis Child 132:929, 1978. Smith DW: Pro and con of the term "anomalad," J PEDIATR 93:160, 1978. Arena JFP, Smith DW: Sex liability to single structural defects, Am J Dis Child 132:970, 1978. Smith DW: Male genital defects in patterns of malformation, Birth Defects 14:57, 1978. Clarren SK, Smith DW, Hanson JW: Helmet treatment for plagiocephaly and congenital muscular torticollis, J PEDIATR 94:43, 1979. Haberkern CM, Smith DW, Jones KL: The "breech head" and its relevance, Am J Dis Child 133:154, 1979. Miller ME, Smith DW: Contruncal malformation complex: Examples of possible monogenic inheritance, Pediatrics 63:890, 1979. Miller ME, Dunn PM, Smith DW: Uterine malformation and fetal deformation, J PED1ATR 94:387, 1979. Pagon RA, Smith DW, Shepard TH: Urethral obstruction malformation complex: A cause of abdominal muscle deficiency and the "prune belly," J PEOIATR 96:900, 1979. Smith DW: Redundant skin folds in the infant: Their origin and relevance, J PEDIATR 94:1021, 1979. Graham JM, Smith DW: Parietal craniotabes in the neonate: Its origin and relevance, J PEDIATR 95:114, 1979. Clarren SK, Smith DW, Harvey MAS, Ward RH, Myrianthopoulos NC: Hypefthermia: A prospective evaluation of a possible teratogenie agent in man, J PEDIATR 95:81, 1979. Miller ME, Fineman R, Smith DW: Postaxial acrofacial dysostosis syndrome, J PEDIATR 95:970, 1979. Graham JM, deSaxe M, Smith DW: Sagittal craniostenosis: Fetal head constraint as one possible cause, J PEDIATR 95:747, 1979. Harvey MAS, Smith DW, Skinner AL: Infant growth standards in relation to parental stature, Clin Pediatr 18:602, 1979. Smith DW: Fetal alcohol syndrome, Hosp Prac 14:121, 1979. Smith DW: Fetal drug syndromes, Pediatr Rev 1:165, 1979. Smith DW: The role of physician in early lethal disorders, Birth Defects 15:123, 1979. Haslam RHA, Smith DW: Autosomal dominant microcephaly, J PEDIATR 95:701, 1979. Schinzel AGL, Smith DW, Miller JR: Monozygotic twinning and structural defects, J PEDIATR 95:921, 1979. Jones KL, Higginbottom MC, Smith DW: Determining role of the optic vesicle in orbital and periocular development and placement, Pediatr Res 14:703, 1980. Graham JM, Badura R J, Smith DW: Coronal craniostenosis: Fetal head constraint as one possible cause, Pediatrics 65:995, 1980. Graham JM, Smith DW: Metopic craniostenosis as a consequence of fetal head constraint: Two interesting experiments of nature, Pediatrics 65:1000, 1980. Graham JM Jr, Miller ME, Stephen M J, Smith DW: Limb reduction anomalies and early inutero limb compression, J PEDIATR 96:1052, 1980. Miller ME, Graham JM Jr, Higginbottom MC, Smith DW: Comprehension-related defects from early amnion rupture:
The Journal of Pediatrics November 1982
Evidence for mechanical teratogenesis, J PED1ATR 98:292, 1981. Graham JM Jr, Hoehn H, Lin MS, Smith DW: Diploid-triploid mixoploidy: Clinical and cytogenetic features, Pediatrics 68:23, 1981. Graham JM, Jr, Higginbottom MC, Smith DW: Preaxial polydactyly of the foot associated with early amnion rupture: Evidence for mechanical teratogenesis, J PEDIATR 98:943, 1981. Pleet H, Graham JM Jr, Smith DW: Central nervous system and facial defects associated with maternal hyperthermia at 4 to 14 weeks' gestation, Pediatrics 67:785, 1981. Graham JM Jr, Smith DW: Dominantly inherited pterygium colli, J PEDtATR 98:664, 1981. Darby BL, Streissguth AP, Smith DW: A preliminary follow-up of 8 children diagnosed fetal alcohol syndrome in infancy, Neurobehav Toxicol Teratol 3:157, 1981. Buffington V, Martin DC, Streissguth AP, Smith DW: Contingent negative variation in fetal alcohol syndrome: Preliminary report, Neurobehav Toxicol Teratol 3:183, 1981. Miller MM, Higginbottom MC, Smith DW: Short umbilical cord: Its origin and relevance, Pediatrics 76:618, 1981. Zerin M, VanAllen MI, Smith DW: Intrinsic auricular muscles and auricular form, Pediatrics 69:91, 1982. Graham JM Jr, Stephens TD, Siebert JR, Smith DW: Determinants in the morphogenesis of muscle tendon insertions, J PEDIATR 101:000, 1982. Stephan M J, Smith DW, Ponzi JW, Allen ER: Scalp vertex aplasia cutis and its origin, J PEDLATR 101:000, 1982.
Smith DW, and Wilson AA: The child with Down's syndrome, Philadelphia, 1973, W. B. Saunders Co. Smith DW: Recognizable patterns of human malformation, ed 2, Philadelphia, 1976, W. B. Saunders Co. Smith DW: Growth and its disorders, Philadelphia, 1977, W. B. Saunders Co. Smith DW, and Marshall RE, editors: Introduction to clinical pediatrics, ed 2, Philadelphia, 1977, W. B. Saunders Co. Smith DW, Bierman EL, and Robinson NM: The biologic ages of man: From conception through old age, ed" 2, Philadelphia, 1978, W. B. Saunders Co. Smith DW, Knight J, and Wood P: Mothering your unborn baby, Philadelphia, 1979, W. B. Saunders Co. Smith DW: The 18 trisomy and 13 trisomy syndromes, in Gardner LI: Endocrine and genetic diseases of childhood, Philadelphia, 1975, W. B. Saunders Co. Smith DW: Fetal alcohol syndrome: A tragic and preventable disorder, in Estes N J, and Heinemann ME: Alcoholism: Development, consequences and intervention, St. Louis, 1977, The C. V. Mosby Co. Smith DW: Growth deficiency dysmorphic syndromes, in Barltrop D: Paediatrics and growth, London, 1978, Fellowship of Postgraduate Medicine. Smith DW: Morphologic syndromes, in Vaughan VC, McKay J, and Bierman E: Textbook of pediatrics, Philadelphia, 1979, W. B. Saunders Co. Smith DW, in Hassell TM, Johnston MC, and Dudley KH: Hydantoin effects on the fetus, New York, 1980, Raven Press.