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American Journal of Medical Genetics|January 1, 1992
Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variantP Franceschini, A Testa, G Bogetti, et al.American Journal of Medical Genetics|January 1, 1992
Deletion of the proximal short arm of chromosome 8R F Stratton, D F Crudo, M Varela, et al.American Journal of Medical Genetics|January 1, 1992
Stable ring chromosome 21: molecular and clinical definition of the lesionT C Falik-Borenstein, T M Pribyl, S M Pulst, et al.American Journal of Medical Genetics|January 1, 1992
Congenital hypothalamic hamartoma syndrome: nosological discussion and minimum diagnostic criteria of a possibly familial formF Encha-Razavi, J C Larroche, J Roume, et al.American Journal of Medical Genetics|January 1, 1992
Agonadism in a 46,XY patient with CHARGE associationT Kushnick, J E Wiley, S M PalmerAmerican Journal of Medical Genetics|July 15, 1992
Cytogenetic, biochemical, and molecular analyses of a 22q13 deletionM C Phelan, G R Thomas, R A Saul, et al.American Journal of Medical Genetics|August 1, 1992
Risk of hepatoblastoma in familial adenomatous polyposisL J Hughes, V V MichelsAmerican Journal of Medical Genetics|October 1, 1990
True precocious puberty in a girl with the fragile X syndromeP S Moore, A E Chudley, J S WinterAmerican Journal of Medical Genetics|June 1, 1990
Oto-palato-digital syndrome, type II: evidence for defective intramembranous ossificationT Ogata, N Matsuo, G Nishimura, et al.American Journal of Medical Genetics|March 1, 1990
Distal deletion of chromosome 1q in an adultF Halal, M Vekemans, P Kaplan, et al.Pageof 854