Showing results (991-1000 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|February 6, 2010
Novel exon nucleotide substitution at the splice junction causes a neonatal Marfan syndromeS-C Chao, J-S Chen, C-H Tsai, et al.
Clinical Genetics|May 1, 1997
MN blood group affects response of serum LDL cholesterol level to a low fat dietA J Birley, R MacLennan, M Wahlqvist, et al.
Clinical Genetics|May 1, 1997
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experienceC Altay, M Alikaşifoglu, A Kara, et al.
Clinical Genetics|May 1, 1997
Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patientK Chrzanowska, M Stumm, M Bialecka, et al.
Clinical Genetics|May 1, 1997
Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patientsA Imamura, Y Suzuki, X Q Song, et al.
Clinical Genetics|May 1, 1997
Pearson marrow pancreas syndrome: a molecular study and clinical managementS Seneca, L De Meirleir, J De Schepper, et al.
Clinical Genetics|May 1, 1997
Brachydactyly in a child with duplication-deficiency subsequent to t(15;20)(q25.2;p12.2)mat. Candidate regions on one or both chromosomes?R A Pfeiffer, C Kändler, E Sieber, et al.
Clinical Genetics|June 1, 1976
Significance of HLA and blood-group incompatibility in spontaneous abortionJ G Lauritsen, J Jøorgensen, F Kissmeyer-Nielsen
Clinical Genetics|April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletionK Devriendt, R Van Hoestenberghe, C Van Hole, et al.
Clinical Genetics|January 1, 1994
Prenatal detection of cri du chat syndrome on uncultured amniocytes using fluorescence in situ hybridization (FISH)M J Pettenati, R Hayworth, K Cox, et al.
Pageof 718