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Table of contents of journal: *American journal of medical genetics

Results: 1-25/753

Authors: Simpson, JL
Citation: Jl. Simpson, Disorders of sexual differentiation, AM J MED G, 89(4), 1999, pp. 175-175

Authors: McElreavey, K Fellous, M
Citation: K. Mcelreavey et M. Fellous, Sex determination and the Y chromosome, AM J MED G, 89(4), 1999, pp. 176-185

Authors: Simpson, JL Rajkovic, A
Citation: Jl. Simpson et A. Rajkovic, Ovarian differentiation and gonadal failure, AM J MED G, 89(4), 1999, pp. 186-200

Authors: Neri, G Opitz, J
Citation: G. Neri et J. Opitz, Syndromal (and nonsyndromal) forms of male pseudohermaphroditism, AM J MED G, 89(4), 1999, pp. 201-209

Authors: Gottlieb, B Pinsky, L Beitel, LK Trifiro, M
Citation: B. Gottlieb et al., Androgen insensitivity, AM J MED G, 89(4), 1999, pp. 210-217

Authors: Belville, C Josso, N Picard, JY
Citation: C. Belville et al., Persistence of mullerian derivatives in males, AM J MED G, 89(4), 1999, pp. 218-223

Authors: Simpson, JL
Citation: Jl. Simpson, Genetics of the female reproductive ducts, AM J MED G, 89(4), 1999, pp. 224-239

Authors: Layman, LC
Citation: Lc. Layman, Genetics of human hypogonadotropic hypogonadism, AM J MED G, 89(4), 1999, pp. 240-248

Authors: Kimberling, WJ
Citation: Wj. Kimberling, Hereditary deafness, AM J MED G, 89(3), 1999, pp. 121-122

Authors: Sundstrom, RA Van Laer, L Van Camp, G Smith, RJH
Citation: Ra. Sundstrom et al., Autosomal recessive nonsyndromic hearing loss, AM J MED G, 89(3), 1999, pp. 123-129

Authors: Cohn, ES Kelley, PM
Citation: Es. Cohn et Pm. Kelley, Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss, AM J MED G, 89(3), 1999, pp. 130-136

Authors: Tranebjaerg, L Bathen, J Tyson, J Bitner-Glindzicz, M
Citation: L. Tranebjaerg et al., Jervell and Lange-Nielsen syndrome: A Norwegian perspective, AM J MED G, 89(3), 1999, pp. 137-146

Authors: Friedman, TB Sellers, JR Avraham, KB
Citation: Tb. Friedman et al., Unconventional myosins and the genetics of hearing loss, AM J MED G, 89(3), 1999, pp. 147-157

Authors: Keats, BJB Corey, DP
Citation: Bjb. Keats et Dp. Corey, The Usher syndromes, AM J MED G, 89(3), 1999, pp. 158-166

Authors: Van Laer, L McGuirt, WT Yang, T Smith, RJH Van Camp, G
Citation: L. Van Laer et al., Autosomal dominant nonsyndromic hearing impairment, AM J MED G, 89(3), 1999, pp. 167-174

Authors: Wilson, GN
Citation: Gn. Wilson, Preventive medicine for genetic disorders, AM J MED G, 89(2), 1999, pp. 55-57

Authors: Schrander-Stumpel, C
Citation: C. Schrander-stumpel, Preconception care: Challenge of the new millennium?, AM J MED G, 89(2), 1999, pp. 58-61

Authors: Msall, ME Tremont, MR
Citation: Me. Msall et Mr. Tremont, Measuring functional status in children with genetic impairments, AM J MED G, 89(2), 1999, pp. 62-74

Authors: Cooley, WC
Citation: Wc. Cooley, Responding to the developmental consequences of genetic conditions: The importance of pediatric primary care, AM J MED G, 89(2), 1999, pp. 75-80

Authors: Clericuzio, CL
Citation: Cl. Clericuzio, Recognition and management of childhood cancer syndromes: A systems approach, AM J MED G, 89(2), 1999, pp. 81-90

Authors: Lovell, CM Saul, RA
Citation: Cm. Lovell et Ra. Saul, Down syndrome clinic in a semi-rural setting, AM J MED G, 89(2), 1999, pp. 91-95

Authors: Spahis, JK Wilson, GN
Citation: Jk. Spahis et Gn. Wilson, Down syndrome: Perinatal complications and counseling experiences in 216 patients, AM J MED G, 89(2), 1999, pp. 96-99

Authors: Van Allen, MI Fung, J Jurenka, SB
Citation: Mi. Van Allen et al., Health care concerns and guidelines for adults with Down syndrome, AM J MED G, 89(2), 1999, pp. 100-110

Authors: Battaglia, A Carey, JC
Citation: A. Battaglia et Jc. Carey, Health supervision and anticipatory guidance of individuals with Wolf-Hirschhorn syndrome, AM J MED G, 89(2), 1999, pp. 111-115

Authors: Barr, M Cohen, MM
Citation: M. Barr et Mm. Cohen, Holoprosencephaly survival and performance, AM J MED G, 89(2), 1999, pp. 116-120
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