Park Spearin Gerald

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Lim BC Park WY Seo EJ Kim KJ Hwang YS Chae JH . De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delay. J Child Neurol. 2011;26:615–618.

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Tenney JR Hopkin RJ Schapiro MB . Deletion of 14-3-3ε and CRK: a clinical syndrome with macrocephaly, developmental delay, and generalized epilepsy. J Child Neurol. 2011;26:223–227.

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Whitehead AS Truedsson L Schneider PM The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypes. Hum Immunol. 1988;21:23–32.

Hersh JH Dale KS Gerald PS Yen FF Weisskopf B Dinno ND . Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding. Am J Dis Child. 1985;139:81–84.

Alper CA Fleischnick E Awdeh Z Extended MHC haplotypes in salt-losing 21-hydroxylase deficiency. Ann N Y Acad Sci. 1985;458:28–35.

Carmi R Meryash DL Wood J Gerald PS . Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infant. Pediatrics. 1984;74:883–886.

Whitehead AS Woods DE Fleischnick E DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex. N Engl J Med. 1984;310:88–91.

Meryash DL Cronk CE Sachs B Gerald PS . An anthropometric study of males with the fragile-X syndrome. Am J Med Genet. 1984;17:159–174.

Gerald PS Grzeschik KH . Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12. Cytogenet Cell Genet. 1984;37:103–126.

Fleischnick E Awdeh ZL Raum D Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients. Lancet. 1983;1:152–156.

Gerald PS . Regionalization of genetic services. Birth Defects Orig Artic Ser. 1983;19:127–133.

Dryja TP Bruns GA Gallie B Low incidence of deletion of the esterase D locus in retinoblastoma patients. Hum Genet. 1983;64:151–155.

Gerald PS Bruns GA . Recombinant DNA and the analysis of cytogenetic disorders associated with mental retardation. Res Publ Assoc Res Nerv Ment Dis. 1983;60:173–179.

Dryja TP Bruns GA Orkin SH Albert DM Gerald PS . Isolation of DNA fragments from chromosome 13. Retina. 1983;3:121–125.

Meryash DL Szymanski LS Gerald PS . Infantile autism associated with the fragile-X syndrome. J Autism Dev Disord. 1982;12:295–301.

Gerald PS Miller OJ . Report of the committee on the genetic constitution of chromosomes 10, 11, and 12. Birth Defects Orig Artic Ser. 1982;18:153–160.

Carmi R Hawley P Wood JW Gerald PS . Hirschsprung disease in progeny of affected individuals: a case report and review of the literature. Birth Defects Orig Artic Ser. 1982;18(3B):187–191.

Gerald PS Miller OJ . Report of the committee on the genetic constitution of chromosomes 10, 11, and 12. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet Cell Genet. 1982;32:153–160.

Gerald PS . X-linked mental retardation and the fragile-X syndrome. Pediatrics. 1981;68:594–595.

Cordero JF Li FP Holmes LB Gerald PS . Wilms tumor in five cousins. Pediatrics. 1980;66:716–719.

Schneeberger EE McCormack J Issenberg HJ Schuster SR Gerald PS . Heterogeneity of ciliary morphology in the immotile-cilia syndrome in man. J Ultrastruct Res. 1980;73:34–43.

Gerald PS . X-linked mental retardation and an X-chromosome marker. N Engl J Med. 1980;303:696–697.

Bruns GA Mintz BJ Leary AC Regina VM Gerald PS . Human lysosomal genes: arylsulfatase A and beta-galactosidase. Biochem Genet. 1979;17:1031–1059.

Gerald PS . The H-Y antigen and male sexual development. N Engl J Med. 1979;300:788–789.

Lubs HA Patil SR Kimberling WJ Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old children. Birth Defects Orig Artic Ser. 1979;15:191–202.

Walzer S Wolff PH Bowen D A method for the longitudinal study of behavioral development in infants and children: the early development of XXY children. J Child Psychol Psychiatry. 1978;19:213–229.

Minna JD Bruns GA Krinsky AH Lalley PA Francke U Gerald PS . Assignment of a Mus musculus gene for triosephosphate isomerase to chromosome 6 and for glyoxalase-I to chromosome 17 using somatic cell hybrids. Somatic Cell Genet. 1978;4:241–252.

Brewster TG Gerald PS . Chromosome disorders associated with mental retardation. Pediatr Ann. 1978;7:82–89.

Walzer S Gerald PS Shah SA . The XYY genotype. Annu Rev Med. 1978;29:568–570.

Gerald PS Bruns GA . Genetic determinants of viral susceptibility. Birth Defects Orig Artic Ser. 1978;14(6A):1–7.

Bruns GA Pierce P Regina VM Gerald PS . Expression of GAPDH and TPI in dog-rodent hybrids. Cytogenet Cell Genet. 1978;22:547–551.

Bruns GA Leary AC Eisenman RE Bazinet CW Regina VM Gerald PS . Expression of ACONS and GALT in man-rodent somatic cell hybrids. Cytogenet Cell Genet. 1978;22:172–176.

Bruns GA Leary AC Regina VM Gerald PS . Lysosomal beta-D-galactosidase in man-hamster somatic cell hybrids. Cytogenet Cell Genet. 1978;22:177–181.

Bruns GA Mintz BJ Leary AC Regina VM Gerald PS . Expression of human arylsulfatase-A in man-hamster somatic cell hybrids. Cytogenet Cell Genet. 1978;22:182–185.

Ingram PH Bruns GA Regina VM Eisenman RE Gerald PS . Expression of alpha-D-mannosidase in man-hamster somatic cell hybrids. Biochem Genet. 1977;15:455–476.

Davidson RL Gerald PS . Induction of mammalian somatic cell hybridization by polyethylene glycol. Methods Cell Biol. 1977;15:325–338.

Patil SR Hecht F Lubs HA Diagnostic radiation and chromosome aberrations. Lancet. 1977;1:151.

Wachtel SS Koo GC Breg WR Serologic detection of a Y-linked gene in XX males and XX true hermaphrodites. N Engl J Med. 1976;295:750–754.

Latt SA Willard HF Gerald PS . BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes. Chromosoma. 1976;57:135–153.

Gerald PS . Editorial: a new frontier for infectious disease research? N Engl J Med. 1976;295:337.

Madan K Allen JW Gerald PS Latt SA . Fluorescence analysis of late DNA replication in mouse metaphase chromosomes using BUdR and 33258 Hoechst. Exp Cell Res. 1976;99:438–444.

Bruns GA Gerald PS . Human glyceraldehyde-3-phosphate dehydrogenase in man-rodent somatic cell hybrids. Science. 1976;192:54–56.

Gerald PS . Sex chromosome disorders. N Engl J Med. 1976;294:706–708.

Gerald PS Walzer S . Statistics and rare phenomena. Science. 1976;193:634.

Davidson RL Gerald PS . Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol. Somatic Cell Genet. 1976;2:165–176.

Bruns GA Gerald PS . Expression of the human adenylate kinase isozymes, phosphopyruvate hydratase, 6-phosphogluconate dehydrogenase, and phosphoglucomutase-1 in man-rodent somatic cell hybrids. Biochem Genet. 1976;14:1–17.

Bruns GA Eisenman RE Gerald PS . Human mitochondrial NADP-dependent isocitrate dehydrogenase in man-mouse somatic cell hybrids. Cytogenet Cell Genet. 1976;17:200–211.

Walzer S Gerald PS . Social class and frequency of XYY and XXY. Science. 1975;190:1228–1229.

Gerald PS. Editorial: Y-linked genes and male-sex determination. N Engl J Med. 1975;293:1095.

Latt SA Stetten G Juergens LA Buchanan GR Gerald PS . Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. Proc Natl Acad Sci U S A. 1975;72:4066–4070.

Gerald PS . Editorial: origin of teratomas. N Engl J Med. 1975;292:103–104.

Latt SA Davidson RL Lin MS Gerald PS . Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 Hoechst. Exp Cell Res. 1974;87:425–429.

Bruns GA Gerald PS . Human acid phosphatase in somatic cell hybrids. Science. 1974;184:480–482.

Gerald PS Brown JA . Proceedings: report of the Committee on the Genetic Constitution of the X Chromosome. Cytogenet Cell Genet. 1974;13:29–34.

Bruns G Gerald PS . Proceedings: the syntenic relationship of the genes for human lysosomal acid phosphatase, isozyme C, and LDH-A. Cytogenet Cell Genet. 1974;13:69–72.

Latt SA Gerald PS . Staining of human metaphase chromosomes with fluorescent conjugates of polylysine. Exp Cell Res. 1973;81:401–406.

Freedom RM Gerald PS . Congenital cardiac disease and the "cat eye" syndrome. Am J Dis Child. 1973;126:16–18.

Kang ES Snodgrass PJ Gerald PS . Ornithine transcarbamylase deficiency in the newborn infant. J Pediatr. 1973;82:642–649.

Kang ES Snodgrass PJ Gerald PS . Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria. Pediatr Res. 1972;6:875–879.

Kang ES Gerald PS . Hyperammonemia and Reye's syndrome. N Engl J Med. 1972;286:1216–1217.

Walzer S Gerald PS . Chromosome abnormalities in 11,154 newborn infants. Am J Hum Genet. 1972;24(6 pt 1):38a.

Feig SA Nathan DG Gerald PS Zarkowski HS . Congenital methemoglobinemia: the result of age-dependent decay of methemoglobin reductase. Blood. 1972;39:407–414.

Gerald PS . Fluorescent staining of human chromosomes. N Engl J Med. 1971;284:788–789.

Sobel RS Tiger A Gerald PS . A second family with the nail-patella allele and the adenylate kinase allele in coupling. Am J Hum Genet. 1971;23:146–149.

Wertelecki W Gerald PS . Clinical and chromosomal studies of the 18q- syndrome. J Pediatr. 1971;78:44–52.

Kang ES Sollee ND Gerald PS . Results of treatment and termination of the diet in phenylketonuria (PKU). Pediatrics. 1970;46:881–890.

Kang ES Gerald PS . Hereditary tyrosinemia and abnormal pyrrole metabolism. J Pediatr. 1970;77:397–406.

Kang ES Gerald PS . Alcaptonuria: rapid semiquantitative determination of homogentisic acid in urine. J Pediatr. 1970;76:939–940.

Kang ES Byers RK Gerald PS . Homocystinuria. Response to pyridoxine. Neurology. 1970;20:503–507.

Hagemeijer AM Gerald PS . Spontaneous hybridization of human leukocytes with a 3T3 (TK-) mouse cell line. Pediatr Res. 1970;4:438.

Brumback R Hagemeijer AM Gerald PS : Monkey-mouse hybrid cell studies. Am J Hum Genet. 1970;22:45a.

Kang ES Kaufman S Gerald PS . Clinical and biochemical observations of patients with atypical phenylketonuria. Pediatrics. 1970;45:83–92.

Necheles TF Allen DM Gerald PS . The many forms of thalassemia: definition and classification of the thalassemia syndromes. Ann N Y Acad Sci. 1969;165:5–12.

Neaves WB Gerald PS . Gene dosage at the lactate dehydrogenase b locus in triploid and diploid teiid lizards. Science. 1969;164:557–559.

Walzer S Breau G Gerald PS . A chromosome survey of 2,400 normal newborn infants. J Pediatr. 1969;74:438–448.

Bloom GE Gerald PS . Localization of genes on chromosome 13: analysis of two kindreds. Am J Hum Genet. 1968;20:495–511.

Say B Gerald PS . A new polydactyly/imperforate-anus/vertebral-anomalies syndrome? Lancet. 1968;2:688.

Neaves WB Gerald PS . Lactate dehydrogenase isozymes in parthenogenetic teiid lizards (Cnemidophorus). Science. 1968;160:1004–1005.

Schwartz E Gerald PS . Mouse hemoglobin: chain composition multiple electrophoretic bands. Experientia. 1967;23:763–765.

Bloom GE Gerald PS Reisman LE . Ring D chromosome: a second case associated with anomalous haptoglobin inheritance. Science. 1967;156:1746–1748.

Gerald PS . The dangers of a successful PKU program. Pediatrics. 1967;39:325–326.

Breau G Walzer S Gerald PS . Karyotype and colchicine exposure time. Lancet. 1967;2:151.

Gerald PS Warner S Singer JD Corcoran PA Umansky I . A ring D chromosome and anomalous inheritance of haptoglobin type. J Pediatr. 1967;70:172–179.

Walzer S Gerald PS Breau G O'Neill D Diamond LK . Hematologic changes in the D1 trisomy syndrome. Pediatrics. 1966;38:419–429.

Walzer S Favara B Ming PM Gerald PS . A new translocation syndrome (3/B). N Engl J Med. 1966;275:290–298.

Bloom GE Gerald PS Diamond LK . Chronic myelogenous leukemia in an infant: serial cytogenetic and fetal hemoglobin studies. Pediatrics. 1966;38:295–299.

Hoefnagel D Gerald PS . Hereditary brachydactyly. Ann Hum Genet. 1966;29:377–382.

Gerald PS Rath CE . Hb C_Georgetown – first abnormal hemoglobin due to two different mutations in the same gene. J Clin Invest. 1966;45:1012.

Bloom GE Warner S Gerald PS Diamond LK . Chromosome abnormalities in constitutional aplastic anemia. N Engl J Med. 1966;274:8–14.

Wertelec W Schindle AM Gerald PS . Partial deletion of chromosome 18. Lancet. 1966;2:641.

Papaspyrou-Zona AV Gerald PS Scott EM . Hereditary methemoglobinemia in Greece. Blood. 1965;25:375–376.

Gerald PS . Genetic determination of hemoglobin structure. Medicine (Baltimore). 1964;43:747–757.

Peetoom F Gerald PS . A simple and inexpensive method for the concentration of protein solutions by means of ultrafiltration. Clin Chim Acta. 1964;10:375–376.

Gerald PS Efron ML . Contributions of a clinical genetics laboratory to the diagnosis and treatment of disease in childhood. Postgrad Med. 1963;34:216–221.

Gerald PS . Chromosome abnormalities. N Engl J Med. 1963;268:1026–1027.

Gerald PS . The clinical implications of hemoglobin structure. Pediatrics. 1963;31:780–785.

Naiman JL Gerald PS . Fetal hemoglobin: improved separation by a modified agar gel electrophoresis. J Lab Clin Med. 1963;61:508–517.

Shahidi NT Gerald PS Diamond LK . Alkali-resistant hemoglobin in aplastic anemia of both acquired and congenital types. N Engl J Med. 1962;266:117–120.

Gerald PS Ingram VM . Recommendations for the nomenclature of hemoglobins. Science. 1961;134:2037.

Gerald PS Ingram VM . Recommendations for the nomenclature of hemoglobins. J Mol Biol. 1961;3:794–795.

Gerald PS Ingram VM . Recommendations for the nomenclature of hemoglobins. Blut. 1961;7:349–350.

Gerald PS Ingram VM . Recommendations for the nomenclature of hemoglobins. J Biol Chem. 1961;236:2155–2156.

Gerald PS Efron ML . Chemical studies of several varieties of Hb M. Proc Natl Acad Sci U S A. 1961;47:1758–1767.

Rausen AR Gerald PS Diamond LK . Genetical evidence for synthesis of transferrin in the foetus. Nature. 1961;192:182.

Rausen AR Gerald PS Diamond LK . Haptoglobin patterns in cord blood serums. Nature. 1961;191:717.

Gammack DB Huehns ER Shooter EM Gerald PS . Identification of the abnormal polypeptide chain of hemoglobin G-Ib. J Mol Biol. 1960;2:372–378.

Pearson HA Gerald PS Diamond LK . Thalassemia intermedia due to interaction of Lepore trait with thalassemia trait; report of three cases. AMA J Dis Child. 1959;97:464–472.

Gerald PS George P . Second spectroscopically abnormal methemoglobin associated with hereditary cyanosis. Science. 1959;129:393–394.

Russell ES Gerald PS . Inherited electrophoretic hemoglobin patterns among 20 inbred strains of mice. Science. 1958;128:1569–1570.

Gerald PS . The electrophoretic and spectroscopic characterization of Hgb M. Blood. 1958;13:936–949.

Gerald PS Diamond LK . A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait. Blood. 1958;13:835–844.

Gerald PS Diamond LK . The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin. Blood. 1958;13:61–69.

Gerald PS Cook CD Diamond LK . Hemoglobin M. Science. 1957;126:300–301.

Andelman MB Gerald PS Rambar AC Kagan BM . Effects of early feeding of strained meat to prematurely born infants. Pediatrics. 1952;9:485–491.

Gerald PS Kagan BM . A method for the determination of gentisic acid in serum. J Biol Chem. 1951;189:467–472.

Kagan BM Jordan DA Gerald PS . Absorption of aqueous dispersions of vitamin A alcohol and vitamin A ester in normal children. J Nutr. 1950;40:275–279.

de la Cruz FF Gerald PS , eds. Trisomy 21 (Down Syndrome): Research Perspectives. Baltimore, MD: University Park Press, 1981.

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