Literature DB >> 1303187

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.

E R Wilcox1, M N Rivolta, B Ploplis, S B Potterf, J Fex.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1992        PMID： 1303187     DOI： 10.1093/hmg/1.3.215-a

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


× No keyword cloud information.
  5 in total

1.  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

2.  Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Authors:  L A Farrer; K S Arnos; J H Asher; C T Baldwin; S R Diehl; T B Friedman; J Greenberg; K M Grundfast; C Hoth; A K Lalwani
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

3.  Homozygosity for Waardenburg syndrome.

Authors:  J Zlotogora; I Lerer; S Bar-David; Z Ergaz; D Abeliovich
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

4.  Evidence for exclusion of a mutation in NRAMP as the cause of familial disseminated atypical mycobacterial infection in a Maltese kindred.

Authors:  M Newport; M Levin; J Blackwell; M A Shaw; R Williamson; C Huxley
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

5.  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
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.