150 related articles for article (PubMed ID: 9342208)
1. Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11.
Bingham PM; Zimmerman RA; McDonald-McGinn D; Driscoll D; Emanuel BS; Zackai E
Am J Med Genet; 1997 Sep; 74(5):538-43. PubMed ID: 9342208
[TBL] [Abstract][Full Text] [Related]
2. Polymicrogyria in chromosome 22q11 deletion syndrome.
Ghariani S; Dahan K; Saint-Martin C; Kadhim H; Morsomme F; Moniotte S; Verellen-Dumoulin C; Sébire G
Eur J Paediatr Neurol; 2002; 6(1):73-7. PubMed ID: 11993959
[TBL] [Abstract][Full Text] [Related]
3. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
Gerkes EH; Hordijk R; Dijkhuizen T; Sival DA; Meiners LC; Sikkema-Raddatz B; van Ravenswaaij-Arts CM
Eur J Med Genet; 2010; 53(5):344-6. PubMed ID: 20553986
[TBL] [Abstract][Full Text] [Related]
4. Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Jawad AF; McDonald-Mcginn DM; Zackai E; Sullivan KE
J Pediatr; 2001 Nov; 139(5):715-23. PubMed ID: 11713452
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 10536461
[TBL] [Abstract][Full Text] [Related]
6. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
Hu Y; Zhu X; Yang Y; Mo X; Sheng M; Yao J; Wang D
Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
[TBL] [Abstract][Full Text] [Related]
7. Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study.
Schaer M; Schmitt JE; Glaser B; Lazeyras F; Delavelle J; Eliez S
Psychiatry Res; 2006 Jan; 146(1):1-11. PubMed ID: 16388934
[TBL] [Abstract][Full Text] [Related]
8. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
Pinquier C; Héron D; de Carvalho W; Lazar G; Mazet P; Cohen D
Encephale; 2001; 27(1):45-50. PubMed ID: 11294038
[TBL] [Abstract][Full Text] [Related]
9. Hypocalcemia and chromosome 22q11 microdeletion.
Garabédian M
Genet Couns; 1999; 10(4):389-94. PubMed ID: 10631928
[TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
McDonald-McGinn DM; Emanuel BS; Zackai EH
Am J Med Genet; 1996 Aug; 64(3):525-6. PubMed ID: 8862635
[No Abstract] [Full Text] [Related]
11. MR of the cerebral operculum: topographic identification and measurement of interopercular distances in healthy infants and children.
Chen CY; Zimmerman RA; Faro S; Parrish B; Wang Z; Bilaniuk LT; Chou TY
AJNR Am J Neuroradiol; 1995 Sep; 16(8):1677-87. PubMed ID: 7502974
[TBL] [Abstract][Full Text] [Related]
12. Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns.
Anaclerio S; Marino B; Carotti A; Digilio MC; Toscano A; Gitto P; Giannotti A; Di Donato R; Dallapiccola B
Ital Heart J; 2001 May; 2(5):384-7. PubMed ID: 11392644
[TBL] [Abstract][Full Text] [Related]
13. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
[TBL] [Abstract][Full Text] [Related]
14. [Cerebral polymicrogyria and 22q11 deletion syndrome].
Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
[TBL] [Abstract][Full Text] [Related]
15. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).
McQuade L; Christodoulou J; Budarf M; Sachdev R; Wilson M; Emanuel B; Colley A
Am J Med Genet; 1999 Sep; 86(1):27-33. PubMed ID: 10440825
[TBL] [Abstract][Full Text] [Related]
16. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
[TBL] [Abstract][Full Text] [Related]
17. Velocardiofacial syndrome (Shprintzen syndrome, chromosome 22q11 deletion syndrome).
Olney AH; Kolodziej P
Ear Nose Throat J; 1998 Jun; 77(6):460-1. PubMed ID: 9674319
[No Abstract] [Full Text] [Related]
18. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
[TBL] [Abstract][Full Text] [Related]
19. The 22q11.2 deletion syndrome.
Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
[TBL] [Abstract][Full Text] [Related]
20. [Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations].
Eirís-Puñal J; Iglesias-Meleiro JM; Blanco-Barca MO; Fuster-Siebert M; Barros-Angueira F; Ansede A; Castro-Gago M
Rev Neurol; 2003 Oct 1-15; 37(7):601-7. PubMed ID: 14582013
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
