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American Journal of Medical Genetics|March 1, 1989
Chediak-Higashi syndrome: prenatal diagnosis by fetal blood examination in the feline model of the diseaseM M Kahraman, D J PrieurAmerican Journal of Medical Genetics|November 1, 1989
Psychological aspects of genetic counseling: VI. A critical review of the literature dealing with education and reproductionS KesslerAmerican Journal of Medical Genetics|August 1, 1986
Restrictive dermopathy: a newly recognized autosomal recessive skin dysplasiaD R Witt, M R Hayden, K A Holbrook, et al.American Journal of Medical Genetics|April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndromeC Patrono, C Rizzo, A Tessa, et al.American Journal of Medical Genetics|April 5, 2000
Intrafamilial phenotypic variability in Engelmann disease (ED): are ED and Ribbing disease the same entity?Y Makita, G Nishimura, S Ikegawa, et al.American Journal of Medical Genetics|February 25, 2000
Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsyK Hallmann, M Durner, T Sander, et al.American Journal of Medical Genetics|February 25, 2000
Potential panic disorder syndrome: clinical and genetic linkage evidenceM M Weissman, A J Fyer, F Haghighi, et al.American Journal of Medical Genetics|February 25, 2000
No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15qM Durner, S Shinnar, S R Resor, et al.American Journal of Medical Genetics|February 25, 2000
Analysis of the serotonin transporter gene linked polymorphism (5-HTTLPR) in anorexia nervosaD Sundaramurthy, L F Pieri, H Gape, et al.American Journal of Medical Genetics|February 25, 2000
Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samplesA M Persico, R Militerni, C Bravaccio, et al.Pageof 854