Genetics of common congenital malformations in man.
作者信息
Carter C O
出版信息
Proc R Soc Med. 1976 Jan;69(1):38-40. doi: 10.1177/003591577606900120.
Abstract
摘要
相似文献
1
Genetics of common congenital malformations in man.人类常见先天性畸形的遗传学
Proc R Soc Med. 1976 Jan;69(1):38-40. doi: 10.1177/003591577606900120.
2
Genetics of common single malformations.常见单发畸形的遗传学
Br Med Bull. 1976 Jan;32(1):21-6. doi: 10.1093/oxfordjournals.bmb.a071318.
3
[Eugenic counseling after a birth of an infant with congenital malformations].[先天性畸形婴儿出生后的优生咨询]
Minerva Med. 1972 Nov 28;63(85):4660-4.
4
Clinical aspects of genetics, the genetics of common malformations and diseases.遗传学的临床方面，常见畸形与疾病的遗传学
Trans Med Soc Lond. 1967;83:84-91.
5
[Role of heredity in the origin of developmental defects].[遗传在发育缺陷起源中的作用]
Cesk Pediatr. 1968 May;23(5):435-7.
6
The genetics of congenital malformations.先天性畸形的遗传学
Proc R Soc Med. 1968 Oct;61(10):991-5. doi: 10.1177/003591576806101015.
7
Genetic factors in congenital malformations. Report of a WHO Scientific Group.先天性畸形中的遗传因素。世界卫生组织科学小组报告。
World Health Organ Tech Rep Ser. 1970;438:1-42.
8
9
[Human genetic counseling. I. Incidence, etiology and risk in repetion of congenital malformations].[人类遗传咨询。I. 先天性畸形复发中的发病率、病因及风险]
Zentralbl Gynakol. 1974 Mar 1;96(9):257-66.
10
Polygenic inheritance of certain common malformations. Evidence and empiric recurrence risk data.某些常见畸形的多基因遗传。证据及经验性复发风险数据。
J Pediatr. 1970 May;76(5):652-9. doi: 10.1016/s0022-3476(70)80282-7.
引用本文的文献
1
PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate.非综合征性唇腭裂中的 PBX-WNT-P63-IRF6 信号通路
Birth Defects Res. 2020 Feb 1;112(3):234-244. doi: 10.1002/bdr2.1630. Epub 2019 Dec 11.
2
Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family.FZD6基因中的调控变异导致一个非裔美国家庭出现非综合征性唇腭裂。
Mol Genet Genomic Med. 2015 Sep;3(5):440-51. doi: 10.1002/mgg3.155. Epub 2015 May 7.
本文引用的文献
1
Genetics of common disorders.常见疾病的遗传学
Br Med Bull. 1969 Jan;25(1):52-7. doi: 10.1093/oxfordjournals.bmb.a070671.
Zotero 插件