Literature DB >> 8588597

Possible homozygous Waardenburg syndrome in a fetus with exencephaly.

S Aymé, N Philip.   

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Year:  1995        PMID： 8588597     DOI： 10.1002/ajmg.1320590227

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


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  4 in total

Review 1.  Waardenburg syndrome.

Authors:  A P Read; V E Newton
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.

Authors:  F A Hol; M P Geurds; S Chatkupt; Y Y Shugart; R Balling; C T Schrander-Stumpel; W G Johnson; B C Hamel; E C Mariman
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

3.  Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret.

Authors:  D Lang; F Chen; R Milewski; J Li; M M Lu; J A Epstein
Journal:  J Clin Invest       Date:  2000-10       Impact factor: 14.808

4.  Restricted Pax3 Deletion within the Neural Tube Results in Congenital Hydrocephalus.

Authors:  Hong-Ming Zhou; Simon J Conway
Journal:  J Dev Biol       Date:  2016-02-01
  4 in total

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