156 related articles for article (PubMed ID: 32154643)
1. Views of adults with 22q11 deletion syndrome on reproductive choices.
McNeill A; Lewis R; Freeth M
Am J Med Genet A; 2020 May; 182(5):1284-1287. PubMed ID: 32154643
[No Abstract] [Full Text] [Related]
2. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.
Meechan DW; Maynard TM; Tucker ES; LaMantia AS
Int J Dev Neurosci; 2011 May; 29(3):283-94. PubMed ID: 20833244
[TBL] [Abstract][Full Text] [Related]
3. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Sullivan KE
Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
[TBL] [Abstract][Full Text] [Related]
4. De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome.
Vittas S; Efstathiou G; Tsakalidis C; Malamaki C; Antari V; Chatzitoliou E; Chatziioannidis I; Galli-Tsinopoulou A; Soubasi V
Cytogenet Genome Res; 2019; 158(1):32-37. PubMed ID: 30799418
[TBL] [Abstract][Full Text] [Related]
5. [Prenatal diagnosis of 22q11 microdeletion syndrome].
Cai M; Huang H; Lin N; Guo N; Wu X; Su L; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):192-195. PubMed ID: 28397216
[TBL] [Abstract][Full Text] [Related]
6. Genetic counseling for the 22q11.2 deletion.
McDonald-McGinn DM; Zackai EH
Dev Disabil Res Rev; 2008; 14(1):69-74. PubMed ID: 18636638
[TBL] [Abstract][Full Text] [Related]
7. Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
McDonald-McGinn DM; Reilly A; Wallgren-Pettersson C; Hoyme HE; Yang SP; Adam MP; Zackai EH; Sullivan KE
Am J Med Genet A; 2006 Apr; 140(8):906-9. PubMed ID: 16532473
[No Abstract] [Full Text] [Related]
8. 22q11.2 Deletion Syndrome: Characterization of Psychosis Spectrum and Future Directions.
Radoeva PD
Biol Psychiatry; 2017 Jul; 82(1):e5-e7. PubMed ID: 28619254
[No Abstract] [Full Text] [Related]
9. Preimplantation genetic diagnosis of DiGeorge syndrome.
Iwarsson E; Ahrlund-Richter L; Inzunza J; Fridström M; Rosenlund B; Hillensjö T; Sjöblom P; Nordenskjöld M; Blennow E
Mol Hum Reprod; 1998 Sep; 4(9):871-5. PubMed ID: 9783847
[TBL] [Abstract][Full Text] [Related]
10. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population.
Kong CW; Cheng YKY; To WWK; Leung TY
Hong Kong Med J; 2019 Feb; 25(1):6-12. PubMed ID: 30655461
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Introduction: advances in research on velo-cardio-facial syndrome/22q11.2 deletion syndrome.
Kates WR; Emanuel BS
Dev Disabil Res Rev; 2008; 14(1):1-2. PubMed ID: 18636630
[No Abstract] [Full Text] [Related]
13. Recognizing a common genetic syndrome: 22q11.2 deletion syndrome.
Kapadia RK; Bassett AS
CMAJ; 2008 Feb; 178(4):391-3. PubMed ID: 18268261
[No Abstract] [Full Text] [Related]
14. A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.
Erickson RP; Díaz de Ståhl T; Bruder CE; Dumanski JP
Am J Med Genet A; 2007 Dec; 143A(24):3302-8. PubMed ID: 18000907
[TBL] [Abstract][Full Text] [Related]
15. Deletion of 22q11 in two brothers with different phenotype.
Kasprzak L; Der Kaloustian VM; Elliott AM; Shevell M; Lejtenyi C; Eydoux P
Am J Med Genet; 1998 Jan; 75(3):288-91. PubMed ID: 9475599
[TBL] [Abstract][Full Text] [Related]
16. Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.
Shetty M; Srikanth A; Kadandale J; Hegde S
Cytogenet Genome Res; 2016; 148(4):249-55. PubMed ID: 27300488
[TBL] [Abstract][Full Text] [Related]
17. Interrupted aortic arch type C associated with DiGeorge syndrome in 22q11.2 deletion: first case detected in Japan.
Fujii I; Ueno Y; Kurano R; Goto Y
Pediatr Int; 2005 Dec; 47(6):698-700. PubMed ID: 16354229
[No Abstract] [Full Text] [Related]
18. The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.
Sullivan KE
Curr Opin Allergy Clin Immunol; 2004 Dec; 4(6):505-12. PubMed ID: 15640691
[TBL] [Abstract][Full Text] [Related]
19. [Molecular basis of microdeletion 22q11].
Bouvagnet P
Arch Pediatr; 2002 May; 9 Suppl 2():97s-99s. PubMed ID: 12108307
[No Abstract] [Full Text] [Related]
20. Prenatal diagnosis of a nasal cyst in association with deletion 22q11 syndrome: a report of two cases.
Karl K; Creton F; Thiel G; Sarioglu N; Heling KS; Chaoui R
Prenat Diagn; 2011 Oct; 31(10):999-1001. PubMed ID: 21710588
[No Abstract] [Full Text] [Related]
[Next] [New Search]
