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Results: 1 to 20 of 27

Related Articles by Review for PubMed (Select 1360769)

1.

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Driscoll DA, Spinner NB, Budarf ML, McDonald-McGinn DM, Zackai EH, Goldberg RB, Shprintzen RJ, Saal HM, Zonana J, Jones MC, et al.

Am J Med Genet. 1992 Sep 15;44(2):261-8.

PMID:
1360769
2.

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

Demczuk S, Lévy A, Aubry M, Croquette MF, Philip N, Prieur M, Sauer U, Bouvagnet P, Rouleau GA, Thomas G, et al.

Hum Genet. 1995 Jul;96(1):9-13. Review.

PMID:
7607662
3.

Velo-cardio-facial syndrome: a review of 120 patients.

Goldberg R, Motzkin B, Marion R, Scambler PJ, Shprintzen RJ.

Am J Med Genet. 1993 Feb 1;45(3):313-9. Review.

PMID:
8434617
4.

Genetic basis of DiGeorge and velocardiofacial syndromes.

Driscoll DA.

Curr Opin Pediatr. 1994 Dec;6(6):702-6. Review.

PMID:
7849818
5.

CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.

Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.

Pathologica. 1999 Jun;91(3):166-72. Review.

PMID:
10536461
6.

The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.

Vantrappen G, Rommel N, Cremers CW, Devriendt K, Frijns JP.

Int J Pediatr Otorhinolaryngol. 1998 Oct 2;45(2):133-41. Review.

PMID:
9849681
7.

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

Portnoï MF, Lebas F, Gruchy N, Ardalan A, Biran-Mucignat V, Malan V, Finkel L, Roger G, Ducrocq S, Gold F, Taillemite JL, Marlin S.

Am J Med Genet A. 2005 Aug 15;137(1):47-51. Review.

PMID:
16007629
8.

Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype.

McLean SD, Saal HM, Spinner NB, Emanuel BS, Driscoll DA.

Am J Dis Child. 1993 Nov;147(11):1212-6. Review.

PMID:
8237917
9.

22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes.

Cuneo BF.

Curr Opin Pediatr. 2001 Oct;13(5):465-72. Review. Erratum in: Curr Opin Pediatr 2002 Apr;14(2):286.

PMID:
11801894
10.
11.

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

Goldmuntz E, Emanuel BS.

Circ Res. 1997 Apr;80(4):437-43. Review.

12.

Annotation: velo-cardio-facial syndrome.

Murphy KC.

J Child Psychol Psychiatry. 2005 Jun;46(6):563-71. Review.

PMID:
15877762
13.

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

Swillen A, Devriendt K, Legius E, Prinzie P, Vogels A, Ghesquière P, Fryns JP.

Genet Couns. 1999;10(1):79-88. Review.

PMID:
10191433
14.

The 22q11.2 deletion syndrome.

Yamagishi H.

Keio J Med. 2002 Jun;51(2):77-88. Review.

15.

Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician.

Thomas JA, Graham JM Jr.

Clin Pediatr (Phila). 1997 May;36(5):253-66. Review.

PMID:
9152551
16.

Velo-cardio-facial syndrome: 30 Years of study.

Shprintzen RJ.

Dev Disabil Res Rev. 2008;14(1):3-10. doi: 10.1002/ddrr.2. Review.

17.

The psychopathological phenotype of velo-cardio-facial syndrome.

Vogels A, Verhoeven WM, Tuinier S, DeVriendt K, Swillen A, Curfs LM, Frijns JP.

Ann Genet. 2002 Apr-Jun;45(2):89-95. Review.

PMID:
12119217
18.

Velo-cardio-facial syndrome: a distinctive behavioral phenotype.

Shprintzen RJ.

Ment Retard Dev Disabil Res Rev. 2000;6(2):142-7. Review.

PMID:
10899808
19.

[Psychiatric disorders in velo-cardio-facial syndrome].

Maesen A, Claes SJ, Neyrinck K.

Tijdschr Psychiatr. 2010;52(1):51-6. Review. Dutch.

20.

Schizophrenia and velo-cardio-facial syndrome.

Murphy KC.

Lancet. 2002 Feb 2;359(9304):426-30. Review.

PMID:
11844533
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