133 related articles for article (PubMed ID: 7633403)
1. Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.
Demczuk S; Aledo R; Zucman J; Delattre O; Desmaze C; Dauphinot L; Jalbert P; Rouleau GA; Thomas G; Aurias A
Hum Mol Genet; 1995 Apr; 4(4):551-8. PubMed ID: 7633403
[TBL] [Abstract][Full Text] [Related]
2. Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome.
Wadey R; Daw S; Taylor C; Atif U; Kamath S; Halford S; O'Donnell H; Wilson D; Goodship J; Burn J
Hum Mol Genet; 1995 Jun; 4(6):1027-33. PubMed ID: 7655455
[TBL] [Abstract][Full Text] [Related]
3. Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene.
Budarf ML; Collins J; Gong W; Roe B; Wang Z; Bailey LC; Sellinger B; Michaud D; Driscoll DA; Emanuel BS
Nat Genet; 1995 Jul; 10(3):269-78. PubMed ID: 7670464
[TBL] [Abstract][Full Text] [Related]
4. Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes.
Demczuk S; Thomas G; Aurias A
Hum Mol Genet; 1996 May; 5(5):633-8. PubMed ID: 8733130
[TBL] [Abstract][Full Text] [Related]
5. Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region.
Goldmuntz E; Wang Z; Roe BA; Budarf ML
Genomics; 1996 Apr; 33(2):271-6. PubMed ID: 8660975
[TBL] [Abstract][Full Text] [Related]
6. Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
Chieffo C; Garvey N; Gong W; Roe B; Zhang G; Silver L; Emanuel BS; Budarf ML
Genomics; 1997 Aug; 43(3):267-77. PubMed ID: 9268629
[TBL] [Abstract][Full Text] [Related]
7. Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.
Taylor C; Wadey R; O'Donnell H; Roberts C; Mattei MG; Kimber WL; Wynshaw-Boris A; Scambler PJ
Mamm Genome; 1997 May; 8(5):371-5. PubMed ID: 9107688
[No Abstract] [Full Text] [Related]
8. A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.
Lindsay EA; Rizzu P; Antonacci R; Jurecic V; Delmas-Mata J; Lee CC; Kim UJ; Scambler PJ; Baldini A
Genomics; 1996 Feb; 32(1):104-12. PubMed ID: 8786095
[TBL] [Abstract][Full Text] [Related]
9. Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.
Sutherland HF; Wadey R; McKie JM; Taylor C; Atif U; Johnstone KA; Halford S; Kim UJ; Goodship J; Baldini A; Scambler PJ
Am J Hum Genet; 1996 Jul; 59(1):23-31. PubMed ID: 8659529
[TBL] [Abstract][Full Text] [Related]
10. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
[TBL] [Abstract][Full Text] [Related]
11. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
Demczuk S; Aurias A
Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827
[TBL] [Abstract][Full Text] [Related]
12. Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.
Holmes SE; Riazi MA; Gong W; McDermid HE; Sellinger BT; Hua A; Chen F; Wang Z; Zhang G; Roe B; Gonzalez I; McDonald-McGinn DM; Zackai E; Emanuel BS; Budarf ML
Hum Mol Genet; 1997 Mar; 6(3):357-67. PubMed ID: 9147638
[TBL] [Abstract][Full Text] [Related]
13. Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.
Lindsay EA; Halford S; Wadey R; Scambler PJ; Baldini A
Genomics; 1993 Aug; 17(2):403-7. PubMed ID: 8406492
[TBL] [Abstract][Full Text] [Related]
14. Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region.
Shiohama A; Sasaki T; Noda S; Minoshima S; Shimizu N
Biochem Biophys Res Commun; 2003 Apr; 304(1):184-90. PubMed ID: 12705904
[TBL] [Abstract][Full Text] [Related]
15. Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region.
Gong W; Emanuel BS; Galili N; Kim DH; Roe B; Driscoll DA; Budarf ML
Hum Mol Genet; 1997 Feb; 6(2):267-76. PubMed ID: 9063747
[TBL] [Abstract][Full Text] [Related]
16. The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.
Wilming LG; Snoeren CA; van Rijswijk A; Grosveld F; Meijers C
Hum Mol Genet; 1997 Feb; 6(2):247-58. PubMed ID: 9063745
[TBL] [Abstract][Full Text] [Related]
17. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11.
Funke B; Saint-Jore B; Puech A; Sirotkin H; Edelmann L; Carlson C; Raft S; Pandita RK; Kucherlapati R; Skoultchi A; Morrow BE
Genomics; 1997 Dec; 46(3):364-72. PubMed ID: 9441739
[TBL] [Abstract][Full Text] [Related]
18. AT-rich palindromes mediate the constitutional t(11;22) translocation.
Edelmann L; Spiteri E; Koren K; Pulijaal V; Bialer MG; Shanske A; Goldberg R; Morrow BE
Am J Hum Genet; 2001 Jan; 68(1):1-13. PubMed ID: 11095996
[TBL] [Abstract][Full Text] [Related]
19. Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
Halford S; Wadey R; Roberts C; Daw SC; Whiting JA; O'Donnell H; Dunham I; Bentley D; Lindsay E; Baldini A
Hum Mol Genet; 1993 Dec; 2(12):2099-107. PubMed ID: 8111380
[TBL] [Abstract][Full Text] [Related]
20. Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome.
Aubry M; Demczuk S; Desmaze C; Aikem M; Aurias A; Julien JP; Rouleau GA
Hum Mol Genet; 1993 Oct; 2(10):1583-7. PubMed ID: 8268910
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]