Literature DB >> 2705472

Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence.

J T Mascarello1, J F Bastian, M C Jones.   

Abstract

We describe a chromosome 22 deletion in a patient with the DiGeorge malformation sequence as manifested by an interrupted aortic arch, mild thymic hypoplasia, and minor craniofacial anomalies. Although others have reported DiGeorge sequence patients with deletions derived from unbalanced translocations involving the chromosome 22 long arm, the small interstitial deletion described here appears to be unusual for patients with this disorder.

Entities:  

Mesh:

Year:  1989        PMID: 2705472     DOI: 10.1002/ajmg.1320320124

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  11 in total

1.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Authors:  D I Wilson; I E Cross; J A Goodship; J Brown; P J Scambler; H H Bain; J F Taylor; K Walsh; A Bankier; J Burn
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

3.  Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome.

Authors:  A M Sharkey; L McLaren; M Carroll; J Fantes; D Green; D Wilson; P J Scambler; H J Evans
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

4.  Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Authors:  K E Sullivan; D McDonald-McGinn; D A Driscoll; B S Emanuel; E H Zackai; A F Jawad
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

Review 5.  Familial interruption of the aortic arch.

Authors:  J W Gobel; M E Pierpont; J H Moller; A Singh; J E Edwards
Journal:  Pediatr Cardiol       Date:  1993-03       Impact factor: 1.655

Review 6.  DiGeorge syndrome: an historical review of clinical and cytogenetic features.

Authors:  F Greenberg
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

7.  Congenital heart disease in CHARGE association.

Authors:  R K Wyse; S al-Mahdawi; J Burn; K Blake
Journal:  Pediatr Cardiol       Date:  1993-03       Impact factor: 1.655

8.  Molecular studies of DiGeorge syndrome.

Authors:  W J Fibison; M Budarf; H McDermid; F Greenberg; B S Emanuel
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

Review 9.  Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.

Authors:  S Demczuk; A Lévy; M Aubry; M F Croquette; N Philip; M Prieur; U Sauer; P Bouvagnet; G A Rouleau; G Thomas
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

10.  Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome.

Authors:  H Kurahashi; K Akagi; K Karakawa; T Nakamura; J P Dumanski; T Sano; S Okada; S Takai; I Nishisho
Journal:  Hum Genet       Date:  1994-03       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.