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G F Cox

Showing results (21-30 of 24) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
American Journal of Human Genetics|September 16, 1999
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.
Journal of Medical Genetics|September 23, 2008
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disordersD T Miller, Y Shen, L A Weiss, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
American Journal of Human Genetics|September 16, 1999
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.
Journal of Medical Genetics|September 23, 2008
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disordersD T Miller, Y Shen, L A Weiss, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
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