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Clinical Genetics|September 1, 1991
Extra small marker chromosome associated with normal phenotype due to 3:1 disjunction of t(14;22) in a parent. Implications for the origin of marker chromosomesK Bröndum-NielsenClinical Genetics|September 1, 1991
Smith-Lemli-Opitz syndrome in female, monozygotic twinsG Tzouvelekis, K Antoniades, A Batma, et al.Clinical Genetics|August 1, 1990
Exclusion mapping of 12 X-linked disease loci and 10 DNA probes from the long arm of the X-chromosomeH M Yang, T Lund, E Niebuhr, et al.Clinical Genetics|May 1, 1990
X-linked myotubular myopathy: a linkage studyC Darnfors, H E Larsson, A Oldfors, et al.Clinical Genetics|September 10, 2009
Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patientsG M Repetto, M L Guzmán, A Puga, et al.Clinical Genetics|September 10, 2009
Identification of 11 novel mutations in USH2A among Japanese patients with Usher syndrome type 2H Nakanishi, M Ohtsubo, S Iwasaki, et al.Clinical Genetics|June 1, 1990
Rate of recombination of chromosomes 21 in parents of children with Down syndromeA J Hamers, H Meyer, R J Jongbloed, et al.Clinical Genetics|January 1, 1991
Coronary artery disease and apolipoprotein A-I/C-III gene polymorphism: a study of Saudi ArabiansK Johansen, B Dunn, J C Tan, et al.Clinical Genetics|December 11, 2008
Severe phenotype with cis-acting heterozygous PMP22 mutationsD Niedrist, F Joncourt, G Mátyás, et al.Clinical Genetics|June 1, 1991
Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84E Blennow, K B NielsenPageof 718