Literature DB >> 7849727

A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region.

J Gabriel1, W Gottlieb, A Garcia, P K Rogan, S Saitoh, R D Nicholls.   

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Year:  1994        PMID： 7849727     DOI： 10.1093/hmg/3.10.1912

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


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  2 in total

1.  A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?

Authors:  K Buiting; B Dittrich; B Dworniczak; I Lerer; D Abeliovich; S Cottrell; I K Temple; J F Harvey; C Lich; S Gross; B Horsthemke
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Authors:  C C Glenn; S Saitoh; M T Jong; M M Filbrandt; U Surti; D J Driscoll; R D Nicholls
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025
  2 in total

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