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R C Trembath

Showing results (81-90 of 86) with videos related to

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Journal of Medical Genetics|December 20, 2003
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasiaR E Harrison, J A Flanagan, M Sankelo, et al.
Journal of Medical Genetics|October 4, 2000
Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta familyJ R Thomson, R D Machado, M W Pauciulo, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
American Journal of Human Genetics|February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndromeJ Kohlhase, P E Taschner, P Burfeind, et al.
Nature|November 4, 2021
MC3R links nutritional state to childhood growth and the timing of pubertyB Y H Lam, A Williamson, S Finer, et al.
Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.
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Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
Journal of Medical Genetics|December 20, 2003
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasiaR E Harrison, J A Flanagan, M Sankelo, et al.
Journal of Medical Genetics|October 4, 2000
Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta familyJ R Thomson, R D Machado, M W Pauciulo, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
American Journal of Human Genetics|February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndromeJ Kohlhase, P E Taschner, P Burfeind, et al.
Nature|November 4, 2021
MC3R links nutritional state to childhood growth and the timing of pubertyB Y H Lam, A Williamson, S Finer, et al.
Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.
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