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American Journal of Medical Genetics|October 23, 1997
Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individualsS B Bleyl, B R Mumford, M C Brown-Harrison, et al.American Journal of Medical Genetics|October 23, 1997
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studiesR Parvari, K J Lei, N Bashan, et al.American Journal of Medical Genetics|October 23, 1997
Cytogenetic analysis of spontaneous abortions: comparison of techniques and assessment of the incidence of confined placental mosaicismD K Griffin, E A Millie, R W Redline, et al.American Journal of Medical Genetics|October 23, 1997
Tetraphocomelia and bilateral cleft lip in a historical case of Roberts syndrome [Virchow, 1898]M Urban, P Rogalla, S Tinschert, et al.American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.American Journal of Medical Genetics|October 23, 1997
Cerebral defects and nephrogenic diabetes insipidus with the ARC syndrome: additional findings or a new syndrome (ARCC-NDI)?R A Coleman, J L Van Hove, C R Morris, et al.American Journal of Medical Genetics|October 23, 1997
Familial transmission of a small supernumerary marker chromosome 8 identified by FISH: an updateH Rothenmund, A E Chudley, A J DawsonAmerican Journal of Medical Genetics|December 1, 1985
Heterozygous cystinuria and urinary lithiasisR Giugliani, I Ferrari, L J GreeneAmerican Journal of Medical Genetics|March 3, 1998
Association between homeobox-containing gene MSX1 and the occurrence of limb deficiencyS J Hwang, T H Beaty, I McIntosh, et al.American Journal of Medical Genetics|March 3, 1998
Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetusN Harada, K Abe, T Nishimura, et al.Pageof 854