Literature DB >> 8401573

Wither polygenic inheritance: mapping Hirschsprung disease.

E Passarge.   

Abstract

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Year:  1993        PMID: 8401573     DOI: 10.1038/ng0893-325

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


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  6 in total

Review 1.  The genetic contribution to the phenotype.

Authors:  U Wolf
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

2.  Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses.

Authors:  E M Santschi; A K Purdy; S J Valberg; P D Vrotsos; H Kaese; J R Mickelson
Journal:  Mamm Genome       Date:  1998-04       Impact factor: 2.957

Review 3.  New perspectives for the elucidation of genetic disorders.

Authors:  Hans-Hilger Ropers
Journal:  Am J Hum Genet       Date:  2007-06-29       Impact factor: 11.025

4.  Single gene disorders come into focus--again.

Authors:  Hans-Hilger Ropers
Journal:  Dialogues Clin Neurosci       Date:  2010       Impact factor: 5.986

Review 5.  Mowat-Wilson syndrome.

Authors:  Livia Garavelli; Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2007-10-24       Impact factor: 4.123

6.  Association between miR-492 rs2289030 G>C and susceptibility to Hirschsprung disease in southern Chinese children.

Authors:  Yi Zheng; Yanqing Liu; Mi Wang; Qiuming He; Xiaoli Xie; Lifeng Lu; Wei Zhong
Journal:  J Int Med Res       Date:  2020-10       Impact factor: 1.671

  6 in total

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