A probable sex difference in mutation rates in ornithine transcarbamylase deficiency-Reference-Cited by-同舟云学术

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A probable sex difference in mutation rates in ornithine transcarbamylase deficiency

Published:1990-01 Issue:2 Volume:84 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bona�ti-Pelli� Catherine,Pelet Anna,Ogier H�l�ne,Nelson Jean-Ren�,Largilli�re Claude,Berthelot Jacques,Saudubray Jean-Marie,Munnich Arnold

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00208933.pdf

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients;Journal of Human Genetics;2007-11-20

2. Late diagnosis of ornithine transcarbamylase defect in three related female patients: Polymorphic presentations;Critical Care Medicine;2002-01

3. Molecular Approaches to the Rett Syndrome Gene;Journal of Child Neurology;1999-12

4. Prenatal diagnosis of ornithine transcarbamylase deficiency;Prenatal Diagnosis;1999-11

5. Ornithine transcarbamylase deficiency: Ten new mutations and high proportion of de novo mutations in heterozygous females;Human Mutation;1997

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