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Human Molecular Genetics|March 1, 1994
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2pR Bashir, T Strachan, S Keers, et al.Human Molecular Genetics|November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosisA Fuchshuber, G Jean, O Gribouval, et al.Journal of Medical Genetics|November 1, 1993
Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish populationB Peral, J L San Millán, C Hernández, et al.The Journal of Biological Chemistry|June 27, 1998
Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2AY Ono, H Shimada, H Sorimachi, et al.Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.Journal De Radiologie|October 10, 2001
[Imaging of primary carcinoid tumor of the pancreas]H Dahan, P Soyer, B Cochand-Priollet, et al.Nature Genetics|February 1, 1997
Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic miceG Gourdon, F Radvanyi, A S Lia, et al.Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|July 1, 1990
Fine-needle aspiration biopsy: an analysis of 89 head and neck casesJ C Platt, D Davidson, C L Nelson, et al.Psychological Medicine|May 1, 1991
Blunting of neuroendocrine responses to infusion of L-tryptophan in women with perimenstrual mood changeJ Bancroft, A Cook, D Davidson, et al.Pageof 96