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Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Reproduction, Nutrition, Development|July 27, 1999
Melatonin synthesis pathway: circadian regulation of the genes encoding the key enzymes in the chicken pineal gland and retinaM Bernard, J Guerlotté, P Grève, et al.
Genetic Testing|May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutationsA L Bernardino, A Ferri, M R Passos-Bueno, et al.
American Journal of Medical Genetics|February 27, 1995
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?S Eggers, V Lauriano, M Melo, et al.
American Journal of Medical Genetics|July 24, 1998
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostosesM R Passos-Bueno, A L Sertié, A Richieri-Costa, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 9, 2001
No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patientsA L Nishimura, J R Oliveira, P A Otto, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1994
[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)]U C Reed, M R Passos-Bueno, S K Nagahashi-Marie, et al.
Neuromuscular Disorders : NMD|April 22, 2004
A novel stop codon mutation in the PMP22 gene associated with a variable phenotypeK T Abe, A M M Lino, M T A Hirata, et al.
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