Literature DB >> 3621644

Deletion of the short arm of chromosome 20.

A M Vianna-Morgante, A Richieri-Costa, C Rosenberg.   

Abstract

A de novo deletion of the short arm of chromosome 20--del (20) (p11) or (p11p13)--is described in a child with psychomotor retardation and multiple congenital anomalies.

Entities:  

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Year:  1987        PMID： 3621644     DOI： 10.1111/j.1399-0004.1987.tb02833.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  4 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.  Familial ring (20) chromosomal mosaicism.

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

3.  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

4.  A Newborn with Panhypopituitarism and Seizures.

Authors:  Trupti Kale; Rachit Patil; Ramesh Pandit
Journal:  Case Rep Genet       Date:  2017-02-01
  4 in total

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