Literature DB >> 6287596

[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)].

J Fraisse, M F Bertheas, F Frère, B Lauras, M O Rolland, C P Brizard.   

Abstract

A karyotype 46,XY,20q-(q13 leads to qter) was found in an infant with severe mental deficiency, epilepsy, and the following dysmorphic features : upward slanting palpebral fissures, hypoplastic nasal bridge, bulbous nose, long philtrum, microretrognathia, and aplasia of the middle phalanx of fingers and toes. Adenosine deaminase activity was within the hemizygous range, permitting regional assignment of the ADA locus to 20q13 leads to qter.

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Year:  1982        PMID: 6287596

Source DB:  PubMed          Journal:  Sem Hop


  3 in total

1.  A novel de novo 20q13.32-q13.33 deletion in a 2-year-old child with poor growth, feeding difficulties and low bone mass.

Authors:  Meena Balasubramanian; Edward Atack; Kath Smith; Michael James Parker
Journal:  J Hum Genet       Date:  2015-03-12       Impact factor: 3.172

2.  A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33.

Authors:  Ryan N Traylor; Damien L Bruno; Trent Burgess; Robert Wildin; Anne Spencer; Devika Ganesamoorthy; David J Amor; Matthew Hunter; Michael Caplan; Jill A Rosenfeld; Aaron Theisen; Beth S Torchia; Lisa G Shaffer; Blake C Ballif; Howard R Slater
Journal:  PLoS One       Date:  2010-08-27       Impact factor: 3.240

3.  Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation.

Authors:  A-C Thuresson; M-L Bondeson; C Edeby; P Ellis; C Langford; J P Dumanski; G Annerén
Journal:  Cytogenet Genome Res       Date:  2007       Impact factor: 1.636

  3 in total

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