Literature DB >> 691837

A partial short arm deletion of chromosome 20:46, XY, del(20)(p11).

K Kogame, T Fukuhara, A Maeda, Y Kudo.   

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Year:  1978        PMID： 691837     DOI： 10.1007/BF02001797

Source DB:  PubMed          Journal:  Jinrui Idengaku Zasshi        ISSN： 0021-5074


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  5 in total

Review 1.  Alagille syndrome and deletion of 20p.

Authors:  F Anad; J Burn; D Matthews; I Cross; B C Davison; R Mueller; M Sands; D M Lillington; E Eastham
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

2.  First trimester abortions associated with a translocation t(1;20)(p36;p11).

Authors:  K Madan; J Kleinhout
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

3.  Familial ring (20) chromosomal mosaicism.

Authors:  E Back; I Voiculescu; M Brünger; G Wolff
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

4.  The gene for bone morphogenetic protein 2A (BMP2A) is localized to human chromosome 20p12 by radioactive and nonradioactive in situ hybridization.

Authors:  V V Rao; C Löffler; J M Wozney; I Hansmann
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

5.  Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome).

Authors:  S Schnittger; C Höfers; P Heidemann; F Beermann; I Hansmann
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132
  5 in total

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