Literature DB >> 10754096

Patients' age at time of testing for chromosome 22q11 microdeletions: missed opportunities for genetic counseling.

Y Liu, S Fallet, R Koppel.   

Abstract

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Year:  2000        PMID： 10754096     DOI： 10.1007/s002469910034

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN： 0172-0643            Impact factor:   1.655


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  7 in total

1.  Deletion 22q11: a newly recognized cause of behavioral and psychiatric disorders.

Authors:  S E McCandless; J A Scott; N H Robin
Journal:  Arch Pediatr Adolesc Med       Date:  1998-05

2.  Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization.

Authors:  C Desmaze; P Scambler; M Prieur; S Halford; D Sidi; F Le Deist; A Aurias
Journal:  Hum Genet       Date:  1993-02       Impact factor: 4.132

3.  Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.

Authors:  S A Webber; E Hatchwell; J C Barber; P E Daubeney; J A Crolla; A P Salmon; B R Keeton; I K Temple; N R Dennis
Journal:  J Pediatr       Date:  1996-07       Impact factor: 4.406

4.  Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.

Authors:  D M McDonald-McGinn; D A Driscoll; B S Emanuel; E Goldmuntz; B J Clark; C Solot; M Cohen; P Schultz; D LaRossa; P Randall; E H Zackai
Journal:  Pediatrics       Date:  1997-05       Impact factor: 7.124

Review 5.  Genetic disorders of cardiac morphogenesis. The DiGeorge and velocardiofacial syndromes.

Authors:  E Goldmuntz; B S Emanuel
Journal:  Circ Res       Date:  1997-04       Impact factor: 17.367

Review 6.  Toward a molecular understanding of congenital heart disease.

Authors:  R M Payne; M C Johnson; J W Grant; A W Strauss
Journal:  Circulation       Date:  1995-01-15       Impact factor: 29.690

7.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Authors:  A K Ryan; J A Goodship; D I Wilson; N Philip; A Levy; H Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; M Prieur; A Aurias; F L Raymond; J Clayton-Smith; E Hatchwell; C McKeown; F A Beemer; B Dallapiccola; G Novelli; J A Hurst; J Ignatius; A J Green; R M Winter; L Brueton; K Brøndum-Nielsen; P J Scambler
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318
  7 in total

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