Literature DB >> 3757303

Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-3pter syndrome.

R M Reifen, R Gale, E Kerem, Y Armon, A Brand, J Dagan, G Kohn.   

Abstract

A male newborn with partial deletion of the short arm of chromosome 3 is described. The patient shares most of the features with the previously reported cases. In addition, cardiac, skeletal and gastrointestinal anomalies not previously reported are described. These characteristics may help in further delineation of the syndrome.

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Year:  1986        PMID： 3757303     DOI： 10.1111/j.1399-0004.1986.tb00581.x

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


  3 in total

1.  Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Authors:  T Drumheller; B C McGillivray; D Behrner; P MacLeod; D E McFadden; J Roberson; C Venditti; K Chorney; M Chorney; D I Smith
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

2.  Double mitral valve, complete atrioventricular canal, and tricuspid atresia in chromosomal 3P-syndrome.

Authors:  A Brand; R M Reifen; Y Armon; E Kerem; E Horenstein; R Gale
Journal:  Pediatr Cardiol       Date:  1987       Impact factor: 1.655

3.  Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH).

Authors:  M E Phipps; E R Maher; N A Affara; F Latif; M A Leversha; M E Ferguson-Smith; Y Nakamura; M Lerman; B Zbar; M A Ferguson-Smith
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132
  3 in total

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