Literature DB >> 4997032

Norrie's disease: an X-linked syndrome of retinal malformation, mental retardation, and deafness.

L B Holmes.   

Abstract

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Year:  1971        PMID： 4997032     DOI： 10.1016/s0022-3476(71)80063-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Advanced bilateral persistent fetal vasculature associated with a novel mutation in the Norrie gene.

Authors:  S Dhingra; D J Shears; V Blake; H Stewart; C K Patel
Journal:  Br J Ophthalmol       Date:  2006-10       Impact factor: 4.638

3.  Norrie's disease: a prospective study of development.

Authors:  H M Goodyear; P M Sonksen; H McConachie
Journal:  Arch Dis Child       Date:  1989-11       Impact factor: 3.791

4.  Norrie disease gene is distinct from the monoamine oxidase genes.

Authors:  K B Sims; L Ozelius; T Corey; W B Rinehart; R Liberfarb; J Haines; W J Chen; R Norio; E Sankila; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

5.  Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeon.

Authors:  Anna I Vickrey; Rebecca Bruders; Zev Kronenberg; Emma Mackey; Ryan J Bohlender; Emily T Maclary; Raquel Maynez; Edward J Osborne; Kevin P Johnson; Chad D Huff; Mark Yandell; Michael D Shapiro
Journal:  Elife       Date:  2018-07-17       Impact factor: 8.140
  5 in total

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