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Clinical Genetics|February 1, 1979
C-band polymorphism in human chromosome no. 6K Madan, A H BruinsmaClinical Genetics|July 1, 1995
Atypical methylmalonic aciduria with progressive encephalopathy, microcephaly and cataract in two siblings--a new recessive syndrome?P Strømme, O Stokke, E Jellum, et al.Clinical Genetics|July 1, 1995
Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart diseaseH K Jensen, P S Hansen, L G Jensen, et al.Clinical Genetics|August 1, 1995
Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemiaH Schuster, C Manke, J Fischer, et al.Clinical Genetics|January 1, 1979
No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45, XO Turner syndromeJ L Burns, J G Hall, E Powers, et al.Clinical Genetics|March 1, 1995
A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3J W Pierpont, D St Jacques, L H Seaver, et al.Clinical Genetics|August 1, 1985
EEC syndrome without ectrodactyly? Report of 8 casesW Küster, F Majewski, P MeineckeClinical Genetics|August 1, 1985
Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritanceH Somer, A Voutilainen, S Knuutila, et al.Pageof 718