XK aprosencephaly may be a new mutation or a dominant genetic defect-Reference-Cited by-同舟云学术

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XK aprosencephaly may be a new mutation or a dominant genetic defect

Published:1989-10 Issue:2 Volume:34 Page:250-250
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Benke Paul J.

Publisher

Wiley

Subject

Genetics (clinical)

Reference8 articles.

1. An update on the holoprosencephalic disorders

2. BD:OAS;Dallaire,1971

3. Single central maxillary incisor and holoprosencephaly

4. Single central maxillary incisor and holoprosencephaly

Cited by 9 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. Cyclopia, aprosencephaly, and acardiac twinning: Is hypoxia-ischemia a unifying mechanism?;American Journal of Medical Genetics Part A;2007-12-15

2. Holoprosencephaly: Clinical, anatomic, and molecular dimensions;Birth Defects Research Part A: Clinical and Molecular Teratology;2006

3. XK-aprosencephaly and related entities;American Journal of Medical Genetics Part A;2005

4. Severe brain and limb defects with possible autosomal recessive inheritance: A series of six cases and review of the literature;American Journal of Medical Genetics;1997-12-12

5. Ring chromosome 13 with loss of the region D13S317-D13S285: Phenotypic overlap with XK syndrome;American Journal of Medical Genetics;1997-10-31

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