500 related articles for article (PubMed ID: 11801894)
21. Noncardiac DiGeorge syndrome diagnosed with multiplex ligation-dependent probe amplification: A case report.
Fu CH; Leung C; Kao CH; Yeh SJ
J Formos Med Assoc; 2015 Aug; 114(8):769-73. PubMed ID: 26254176
[TBL] [Abstract][Full Text] [Related]
22. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.
Wang JL; Chen SJ; Chung MY; Niu DM; Lin CY; Hwang BT; Lu JH
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(5):385-9. PubMed ID: 9401184
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes.
Sullivan KE; Jawad AF; Randall P; Driscoll DA; Emanuel BS; McDonald-McGinn DM; Zackai EH
Clin Immunol Immunopathol; 1998 Feb; 86(2):141-6. PubMed ID: 9473376
[TBL] [Abstract][Full Text] [Related]
27. Microdeletion 22q11 and oesophageal atresia.
Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
[TBL] [Abstract][Full Text] [Related]
28. 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; 137(1):47-51. PubMed ID: 16007629
[TBL] [Abstract][Full Text] [Related]
29. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome].
Hjalgrim H; Hahnemann JM; Timshel S; Brøndum-Nielsen K
Ugeskr Laeger; 2000 Jul; 162(31):4169-70. PubMed ID: 10962926
[No Abstract] [Full Text] [Related]
30. Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.
Unolt M; DiCairano L; Schlechtweg K; Barry J; Howell L; Kasperski S; Nance M; Adzick NS; Zackai EH; McDonald-McGinn DM
Am J Med Genet A; 2017 Jan; 173(1):135-142. PubMed ID: 27682988
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.
Marino B; Digilio MC; Toscano A; Giannotti A; Dallapiccola B
Genet Couns; 1999; 10(1):25-33. PubMed ID: 10191426
[TBL] [Abstract][Full Text] [Related]
33. Microdeletion 22q11 in complex cardiovascular malformations.
Mehraein Y; Wippermann CF; Michel-Behnke I; Nhan Ngo TK; Hillig U; Giersberg M; Aulepp U; Barth H; Fritz B; Rehder H
Hum Genet; 1997 Apr; 99(4):433-42. PubMed ID: 9099830
[TBL] [Abstract][Full Text] [Related]
34. [Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients].
Levy-Mozziconacci A; Lacombe D; Leheup B; Wernert F; Rouault F; Philip N
Arch Pediatr; 1996 Aug; 3(8):761-8. PubMed ID: 8998528
[TBL] [Abstract][Full Text] [Related]
35. An adult case of 22q11.2 deletion syndrome diagnosed in a 36-year-old woman with hypocalcemia caused by hypoparathyroidism and Hashimoto's thyroiditis.
Nakada Y; Terui K; Kageyama K; Tsushima Y; Murakami H; Soma Y; Nigawara T; Sakihara S
Intern Med; 2013; 52(12):1365-8. PubMed ID: 23774548
[TBL] [Abstract][Full Text] [Related]
36. Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician.
Thomas JA; Graham JM
Clin Pediatr (Phila); 1997 May; 36(5):253-66. PubMed ID: 9152551
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. Associated anomalies in asymmetric crying facies and 22q11 deletion.
Akcakus M; Ozkul Y; Gunes T; Kurtoglu S; Cetin N; Kisaarslan AP; Dundar M
Genet Couns; 2003; 14(3):325-30. PubMed ID: 14577677
[TBL] [Abstract][Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
