128 related articles for article (PubMed ID: 8786095)
1. 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]
2. 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]
3. 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]
4. 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]
5. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
Funke B; Pandita RK; Morrow BE
Genomics; 2001 May; 73(3):264-71. PubMed ID: 11350118
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.
Boultwood J; Fidler C; Strickson AJ; Watkins F; Kostrzewa M; Jaju RJ; Müller U; Wainscoat JS
Genomics; 2000 May; 66(1):26-34. PubMed ID: 10843801
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
Funke B; Puech A; Saint-Jore B; Pandita R; Skoultchi A; Morrow B
Genomics; 1998 Oct; 53(2):146-54. PubMed ID: 9790763
[TBL] [Abstract][Full Text] [Related]
10. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB
Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.
Lund J; Chen F; Hua A; Roe B; Budarf M; Emanuel BS; Reeves RH
Genomics; 2000 Feb; 63(3):374-83. PubMed ID: 10704284
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene.
Chatterjee TK; Eapen A; Kanis AB; Fisher RA
Genomics; 1997 Oct; 45(2):429-33. PubMed ID: 9344672
[TBL] [Abstract][Full Text] [Related]
15. A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p).
Baens M; Wlodarska I; Corveleyn A; Hoornaert I; Hagemeijer A; Marynen P
Genomics; 1999 Feb; 56(1):40-50. PubMed ID: 10036184
[TBL] [Abstract][Full Text] [Related]
16. Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes.
Seranski P; Heiss NS; Dhorne-Pollet S; Radelof U; Korn B; Hennig S; Backes E; Schmidt S; Wiemann S; Schwarz CE; Lehrach H; Poustka A
Genomics; 1999 Feb; 56(1):1-11. PubMed ID: 10036180
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Cloning of a novel human neural cell adhesion molecule gene (NCAM2) that maps to chromosome region 21q21 and is potentially involved in Down syndrome.
Paoloni-Giacobino A; Chen H; Antonarakis SE
Genomics; 1997 Jul; 43(1):43-51. PubMed ID: 9226371
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. DiGeorge anomaly and chromosome 10p deletions: one or two loci?
Dasouki M; Jurecic V; Phillips JA; Whitlock JA; Baldini A
Am J Med Genet; 1997 Nov; 73(1):72-5. PubMed ID: 9375926
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]