Literature DB >> 4078871

Partial 2p deletion in a girl with a complex chromosome rearrangement involving chromosomes 2, 6, 11, and 21.

R S Young, M A Medrano, K L Hansen.   

Abstract

We describe the clinical and cytogenetic findings of a 9 1/2 month old girl with a complex chromosome rearrangement resulting in a probable deletion of band 2p14. She does not resemble other reported cases of del(2p).

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Year:  1985        PMID： 4078871      PMCID： PMC1049489          DOI： 10.1136/jmg.22.5.401

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  5 in total

1.  Deletion of the short arm of chromosome 2 from a subject with congenital anomalies. Repository identification no. GM-1138.

Authors:  E Zackai; B Emanuel; W J Mellman; M M Aronson; B Bozarth; A E Greene; L L Coriell
Journal:  Cytogenet Cell Genet       Date:  1977

2.  Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2.

Authors:  M A Ferguson-Smith; B F Newman; P M Ellis; D M Thomson; I D Riley
Journal:  Nat New Biol       Date:  1973-06-27

3.  Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata.

Authors:  J P Fryns; P De Waele; H Van Den Berghe
Journal:  Hum Genet       Date:  1979-10-01       Impact factor: 4.132

4.  Interstitial deletion (2)(p13p15).

Authors:  D Duca; D Ioan; P Meilă; M Ionescu-Cerna; L Simionescu; C Maximilian
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23.

Authors:  B S Emanuel; E H Zackai; D C Van Dyke; D M Swallow; F H Allen; W J Mellman
Journal:  Am J Med Genet       Date:  1979
  5 in total
  1 in total

1.  De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data.

Authors:  F J Los; J O Van Hemel; H J Jacobs; S L Drop; J J van Dongen
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318
  1 in total

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