Literature DB >> 4039891

X-linked midline defects.

H V Toriello, J V Higgins.   

Abstract

Opitz and Gilbert [Am J Med Genet 12:443-455, 1982] have postulated that the midline may be a kind of developmental field. Although developmental field defects (primary malformations) usually occur sporadically, in some instances they can be caused by a single gene mutation. We report on a family in which the occurrence of midline defects was consistent with X-linked inheritance. Anomalies present in the family include hydrocephalus, anencephaly, cleft lip, congenital heart defect, renal agenesis, and hypospadias.

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Year:  1985        PMID: 4039891     DOI: 10.1002/ajmg.1320210121

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


  3 in total

1.  The epidemiology of congenital abnormalities of the central nervous system in children.

Authors:  I P Minkov
Journal:  Neurosci Behav Physiol       Date:  1993 Jan-Feb

2.  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

3.  Pentalogy of Cantrell associated with hypoplastic left heart syndrome.

Authors:  D S Wheeler; J D St Louis
Journal:  Pediatr Cardiol       Date:  2007-06-11       Impact factor: 1.838

  3 in total

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