Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2-Reference-Cited by-同舟云学术

Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2

Published:2012-01-13 Issue:2 Volume:158A Page:309-314
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Tompson Stuart W.,Faqeih Eissa Ali,Ala-Kokko Leena,Hecht Jacqueline T.,Miki Rika,Funari Tara,Funari Vincent A.,Nevarez Lisette,Krakow Deborah,Cohn Daniel H.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

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2. Recurrence of fibrochondrogenesis in a consanguineous family;Al-Gazali;Clin Dysmorphol,1999

3. Fibrochondrogenesis in male twins at 24 weeks gestation;Bankier;Am J Med Genet,1991

4. Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus;Chen;J Med Genet,2005

5. Detection of a de novo R1066H mutation in an Italian patient affected with cystic fibrosis;Cremonesi;Hum Genet,1996

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