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Gerd Scherer

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American Journal of Human Genetics|December 11, 2008

TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndromeEkkehart Lausch, Pia Hermanns, Henner F Farin, et al.

Human Molecular Genetics|September 13, 2015

FGFR2 mutation in 46,XY sex reversal with craniosynostosisStefan Bagheri-Fam, Makoto Ono, Li Li, et al.

Development (Cambridge, England)|May 12, 2009

The PGD2 pathway, independently of FGF9, amplifies SOX9 activity in Sertoli cells during male sexual differentiationBrigitte Moniot, Faustine Declosmenil, Francisco Barrionuevo, et al.

Journal of Medical Genetics|January 22, 2015

Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex developmentGwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.

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Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 44 results.

American Journal of Human Genetics|December 11, 2008

TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndromeEkkehart Lausch, Pia Hermanns, Henner F Farin, et al.

Human Molecular Genetics|September 13, 2015

FGFR2 mutation in 46,XY sex reversal with craniosynostosisStefan Bagheri-Fam, Makoto Ono, Li Li, et al.

Development (Cambridge, England)|May 12, 2009

The PGD2 pathway, independently of FGF9, amplifies SOX9 activity in Sertoli cells during male sexual differentiationBrigitte Moniot, Faustine Declosmenil, Francisco Barrionuevo, et al.

Journal of Medical Genetics|January 22, 2015

Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex developmentGwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.

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