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American Journal of Medical Genetics|March 17, 2001
Mutations in the caveolin-3 gene: When are they pathogenic?F de Paula, M Vainzof, A L Bernardino, et al.American Journal of Medical Genetics|March 17, 2001
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlationA Rauch, S Schellmoser, C Kraus, et al.American Journal of Medical Genetics|April 6, 1999
Oral-facial-digital syndrome with hypothalamic hamartoma, postaxial ray hypoplasia of the limbs, and vagino-cystic communication: a new variant?I Fujiwara, Y Kondo, K IinumaAmerican Journal of Medical Genetics|April 6, 1999
Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: a new MCA/MR syndrome?A Mégarbané, S Haddad-Zebouni, R Nabbout, et al.American Journal of Medical Genetics|April 6, 1999
Mutchinick syndrome in a Japanese girlH Tonoki, T Hattori, H Kamoshida, et al.American Journal of Medical Genetics|April 6, 1999
Congenital malformations in twins: an international studyP Mastroiacovo, E E Castilla, C Arpino, et al.American Journal of Medical Genetics|April 5, 2000
Homogeneity of the age at diagnosis in sibs with Type 2 diabetes: implications for sib-pair analysisA Lev-Ran, E Sprecher, Y Yerushalmy, et al.American Journal of Medical Genetics|June 27, 2000
Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X allelesL A Larsen, J S Armstrong, K Grønskov, et al.American Journal of Medical Genetics|June 27, 2000
Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotesV Drasinover, S Ehrlich, N Magal, et al.American Journal of Medical Genetics|March 8, 2000
Familial occurrence of isolated right ventricular hypoplasiaM Chessa, S Redaelli, G Masszi, et al.Pageof 854