579 related articles for article (PubMed ID: 7901419)
1. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
Goldmuntz E; Driscoll D; Budarf ML; Zackai EH; McDonald-McGinn DM; Biegel JA; Emanuel BS
J Med Genet; 1993 Oct; 30(10):807-12. PubMed ID: 7901419
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
Driscoll DA; Salvin J; Sellinger B; Budarf ML; McDonald-McGinn DM; Zackai EH; Emanuel BS
J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155
[TBL] [Abstract][Full Text] [Related]
3. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
[TBL] [Abstract][Full Text] [Related]
4. Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.
Takahashi K; Kido S; Hoshino K; Ogawa K; Ohashi H; Fukushima Y
Eur J Pediatr; 1995 Nov; 154(11):878-81. PubMed ID: 8582397
[TBL] [Abstract][Full Text] [Related]
5. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.
McDonald-McGinn DM; Driscoll DA; Emanuel BS; Goldmuntz E; Clark BJ; Solot C; Cohen M; Schultz P; LaRossa D; Randall P; Zackai EH
Pediatrics; 1997 May; 99(5):E9. PubMed ID: 9113966
[TBL] [Abstract][Full Text] [Related]
6. Genetic basis of DiGeorge and velocardiofacial syndromes.
Driscoll DA
Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 10536461
[TBL] [Abstract][Full Text] [Related]
8. Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183).
Mulder MP; Wilke M; Langeveld A; Wilming LG; Hagemeijer A; van Drunen E; Zwarthoff EC; Riegman PH; Deelen WH; van den Ouweland AM
Hum Genet; 1995 Aug; 96(2):133-41. PubMed ID: 7635459
[TBL] [Abstract][Full Text] [Related]
9. Clinical correlation of chromosome 22q11.2 fluorescent in situ hybridization analysis and velocardiofacial syndrome.
Oh AK; Workman LA; Wong GB
Cleft Palate Craniofac J; 2007 Jan; 44(1):62-6. PubMed ID: 17214538
[TBL] [Abstract][Full Text] [Related]
10. Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.
Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
Am J Med Genet; 1994 Oct; 52(4):445-9. PubMed ID: 7747757
[TBL] [Abstract][Full Text] [Related]
11. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
[TBL] [Abstract][Full Text] [Related]
12. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
Kelly D; Goldberg R; Wilson D; Lindsay E; Carey A; Goodship J; Burn J; Cross I; Shprintzen RJ; Scambler PJ
Am J Med Genet; 1993 Feb; 45(3):308-12. PubMed ID: 8434616
[TBL] [Abstract][Full Text] [Related]
13. Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion.
Debrus S; Berger G; de Meeus A; Sauer U; Guillaumont S; Voisin M; Bozio A; Demczuk S; Aurias A; Bouvagnet P
Hum Genet; 1996 Feb; 97(2):138-44. PubMed ID: 8566942
[TBL] [Abstract][Full Text] [Related]
14. 22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes.
Cuneo BF
Curr Opin Pediatr; 2001 Oct; 13(5):465-72. PubMed ID: 11801894
[TBL] [Abstract][Full Text] [Related]
15. Congenital cardiac defects with 22q11 deletion.
Giray O; Ulgenalp A; Bora E; Sağin Saylam G; Unal N; Meşe T; Hüdaoğlu S; Erçal D
Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
[TBL] [Abstract][Full Text] [Related]
16. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients.
Borgmann S; Luhmer I; Arslan-Kirchner M; Kallfelz HC; Schmidtke J
Eur J Pediatr; 1999 Dec; 158(12):958-63. PubMed ID: 10592069
[TBL] [Abstract][Full Text] [Related]
17. 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin.
Fokstuen S; Arbenz U; Artan S; Dutly F; Bauersfeld U; Brecevic L; Fasnacht M; Röthlisberger B; Schinzel A
Clin Genet; 1998 Jan; 53(1):63-9. PubMed ID: 9550365
[TBL] [Abstract][Full Text] [Related]
18. Cardiac Registry screening for DiGeorge Critical Region deletion using loss of heterozygosity analysis.
Katzman PJ; Smoot LB; Cox GF
Pediatr Dev Pathol; 2006; 9(4):266-79. PubMed ID: 16944986
[TBL] [Abstract][Full Text] [Related]
19. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
[TBL] [Abstract][Full Text] [Related]
20. Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2.
Li M; Zackai EH; Niikawa N; Kaplan P; Driscoll DA
Am J Med Genet; 1996 Oct; 65(2):101-3. PubMed ID: 8911598
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
