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V Brancolini

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Acta Neuropathologica|August 1, 1996

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, S Palmeri, et al.

American Journal of Human Genetics|November 5, 1997

The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative casesH C Tsou, D H Teng, X L Ping, et al.

Science (New York, N.Y.)|February 21, 1998

Alopecia universalis associated with a mutation in the human hairless geneW Ahmad, M Faiyaz ul Haque, V Brancolini, et al.

American Journal of Human Genetics|January 23, 1999

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition diseaseL J Andrew, V Brancolini, L S de la Pena, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Acta Neuropathologica|August 1, 1996

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, S Palmeri, et al.

American Journal of Human Genetics|November 5, 1997

The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative casesH C Tsou, D H Teng, X L Ping, et al.

Science (New York, N.Y.)|February 21, 1998

Alopecia universalis associated with a mutation in the human hairless geneW Ahmad, M Faiyaz ul Haque, V Brancolini, et al.

American Journal of Human Genetics|January 23, 1999

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition diseaseL J Andrew, V Brancolini, L S de la Pena, et al.

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