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Hiroshi Kitoh

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American Journal of Medical Genetics. Part A|July 13, 2006

Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypesHaruya Sakai, Remco Visser, Shiro Ikegawa, et al.

American Journal of Human Genetics|May 14, 2013

Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disordersMasahiro Nakajima, Shuji Mizumoto, Noriko Miyake, et al.

American Journal of Human Genetics|June 21, 2011

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasiasCarine Le Goff, Clémentine Mahaut, Lauren W Wang, et al.

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Search research articles

Showing results (131-140 of 133) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 133 results.

American Journal of Medical Genetics. Part A|July 13, 2006

Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypesHaruya Sakai, Remco Visser, Shiro Ikegawa, et al.

American Journal of Human Genetics|May 14, 2013

Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disordersMasahiro Nakajima, Shuji Mizumoto, Noriko Miyake, et al.

American Journal of Human Genetics|June 21, 2011

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasiasCarine Le Goff, Clémentine Mahaut, Lauren W Wang, et al.

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