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P I Patel

Showing results (81-90 of 85) with videos related to

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Nature Genetics|June 1, 1992
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1AP I Patel, B B Roa, A A Welcher, et al.
Cell|July 26, 1991
DNA duplication associated with Charcot-Marie-Tooth disease type 1AJ R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.
Human Genetics|December 1, 1996
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patientsB J Trask, H Mefford, G van den Engh, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
Nature Genetics|June 1, 1992
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1AP I Patel, B B Roa, A A Welcher, et al.
Cell|July 26, 1991
DNA duplication associated with Charcot-Marie-Tooth disease type 1AJ R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.
Human Genetics|December 1, 1996
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patientsB J Trask, H Mefford, G van den Engh, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
Pageof 9