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The Journal of Clinical Investigation|March 1, 1994
Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotypeM R Pollak, Y H Chou, S J Marx, et al.
American Journal of Human Genetics|June 19, 1998
Amerindian pyruvate carboxylase deficiency is associated with two distinct missense mutationsM A Carbone, N MacKay, M Ling, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 1998
The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3H Jüppner, E Schipani, M Bastepe, et al.
American Journal of Human Genetics|February 17, 2001
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancerH A Risch, J R McLaughlin, D E Cole, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 2, 2001
Comparison of breast magnetic resonance imaging, mammography, and ultrasound for surveillance of women at high risk for hereditary breast cancerE Warner, D B Plewes, R S Shumak, et al.
American Journal of Human Genetics|October 27, 1997
Differential structuring of human populations for homologous X and Y microsatellite lociR Scozzari, F Cruciani, P Malaspina, et al.
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