Literature DB >> 2877437

An anonymous X-chromosomal clone identifying a frequent RFLP at Xp21-22 (HGM8 provisional no. DXS207).

P Ahrens, T A Kruse.   

Abstract

Mesh：

Year:  1986        PMID： 2877437      PMCID： PMC311809          DOI： 10.1093/nar/14.19.7819

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  4 in total

1.  Linkage relationships and gene order around the locus for X-linked retinoschisis.

Authors:  T Alitalo; H Forsius; J Kärnä; R R Frants; A W Eriksson; S Wood; T A Kruse; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

2.  DNA linkage analysis of X-linked retinoschisis.

Authors:  N Dahl; P Goonewardena; J Chotai; M Anvret; U Pettersson
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

3.  Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.

Authors:  A Sefiani; D Sinnett; L Abel; S Szpiro-Tapia; S Heuertz; I Craig; N Fraser; T A Kruse; M Frydman; M O Peter
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

4.  Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome.

Authors:  D Zhu; D M Alcorn; S E Antonarakis; L S Levin; P C Huang; T N Mitchell; A C Warren; I H Maumenee
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132
  4 in total

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