Literature DB >> 8839734

The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease.

K Devriendt, B Eyskens, A Swillen, M Dumoulin, M Gewillig, J P Fryns.   

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Year:  1996        PMID： 8839734     DOI： 10.1007/bf01957162

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  7 in total

1.  Tetralogy of Fallot associated with chromosome 22q11 deletion.

Authors:  K Momma; C Kondo; M Ando; R Matsuoka; A Takao
Journal:  Am J Cardiol       Date:  1995-09-15       Impact factor: 2.778

2.  Prediction of persistent immunodeficiency in the DiGeorge anomaly.

Authors:  J Bastian; S Law; L Vogler; A Lawton; H Herrod; S Anderson; S Horowitz; R Hong
Journal:  J Pediatr       Date:  1989-09       Impact factor: 4.406

3.  Deletions within chromosome 22q11 in familial congenital heart disease.

Authors:  D I Wilson; J A Goodship; J Burn; I E Cross; P J Scambler
Journal:  Lancet       Date:  1992-09-05       Impact factor: 79.321

4.  Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).

Authors:  R Wadey; S Daw; A Wickremasinghe; C Roberts; D Wilson; J Goodship; J Burn; S Halford; P J Scambler
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

5.  Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.

Authors:  K Takahashi; S Kido; K Hoshino; K Ogawa; H Ohashi; Y Fukushima
Journal:  Eur J Pediatr       Date:  1995-11       Impact factor: 3.183

6.  Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

Authors:  B Morrow; R Goldberg; C Carlson; R Das Gupta; H Sirotkin; J Collins; I Dunham; H O'Donnell; P Scambler; R Shprintzen
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

7.  Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.

Authors:  E A Lindsay; R Goldberg; V Jurecic; B Morrow; C Carlson; R S Kucherlapati; R J Shprintzen; A Baldini
Journal:  Am J Med Genet       Date:  1995-07-03
  7 in total
  4 in total

1.  Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defects.

Authors:  F L Raymond; J M Simpson; C M Mackie; G K Sharland
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

Review 2.  Transcription factor pathways and congenital heart disease.

Authors:  David J McCulley; Brian L Black
Journal:  Curr Top Dev Biol       Date:  2012       Impact factor: 4.897

3.  Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Authors:  A Swillen; K Devriendt; E Legius; B Eyskens; M Dumoulin; M Gewillig; J P Fryns
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

4.  Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.

Authors:  Yue-Juan Xu; Jian Wang; Rang Xu; Peng-Jun Zhao; Xi-Ke Wang; Heng-Juan Sun; Li-Ming Bao; Jie Shen; Qi-Hua Fu; Fen Li; Kun Sun
Journal:  BMC Med Genet       Date:  2011-12-21       Impact factor: 2.103
  4 in total

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