Literature DB >> 2333913

Evidence for a major gene in familial anencephaly.

L G Shaffer1, M L Marazita, J Bodurtha, A Newlin, W E Nance.   

Abstract

A 21-year-old white woman sought counseling after the birth of two consecutive anencephalic male fetuses with complete rachischisis and discordant renal dysplasia. The presence of parental consanguinity prompted reconsideration of recessive inheritance. The segregation ratio from 23 additional consanguineous cases was compared with that observed in 294 presumably nonconsanguineous families previously reported. Using classical segregation analysis, the segregation ratios in the non-sporadic cases were consistent with a major autosomal recessive locus in both populations.

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Year:  1990        PMID: 2333913     DOI: 10.1002/ajmg.1320360119

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

Review 1.  Genetic epidemiology of neural tube defects.

Authors:  Philip J Lupo; A J Agopian; Heidi Castillo; Jonathan Castillo; Gerald H Clayton; Nienke P Dosa; Betsy Hopson; David B Joseph; Brandon G Rocque; William O Walker; John S Wiener; Laura E Mitchell
Journal:  J Pediatr Rehabil Med       Date:  2017-12-11

2.  Genetic study of indirect inguinal hernia.

Authors:  Y Gong; C Shao; Q Sun; B Chen; Y Jiang; C Guo; J Wei; Y Guo
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

3.  The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.

Authors:  G N Kavaslar; S Onengüt; O Derman; A Kaya; A Tolun
Journal:  Am J Hum Genet       Date:  2000-04-04       Impact factor: 11.025

4.  Mapping a chromosomal locus for valproic acid-induced exencephaly in mice.

Authors:  Yunxia Wang Lundberg; Robert M Cabrera; Kimberly A Greer; Jian Zhao; Rohit Garg; Richard H Finnell
Journal:  Mamm Genome       Date:  2004-05       Impact factor: 2.957

5.  Absence of linkage between familial neural tube defects and PAX3 gene.

Authors:  S Chatkupt; F A Hol; Y Y Shugart; M P Geurds; E S Stenroos; M R Koenigsberger; B C Hamel; W G Johnson; E C Mariman
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

  5 in total

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