De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome-Reference-Cited by-同舟云学术

De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome

Published:1999-02 Issue:2 Volume:64 Page:446-461
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Oldridge Michael,Zackai Elaine H.,McDonald-McGinn Donna M.,Iseki Sachiko,Morriss-Kay Gillian M.,Twigg Stephen R.F.,Johnson David,Wall Steven A.,Jiang Wen,Theda Christiane,Jabs Ethylin Wang,Wilkie Andrew O.M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference60 articles.

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3. The feet in Pfeiffer's syndrome;Anderson;J Craniofac Surg,1998

4. Standardized nomenclature for Alu repeats;Batzer;J Mol Evol,1996

5. Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeats;Batzer;J Mol Biol,1995

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