221 related articles for article (PubMed ID: 15750894)
1. Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.
Klaassens M; van Dooren M; Eussen HJ; Douben H; den Dekker AT; Lee C; Donahoe PK; Galjaard RJ; Goemaere N; de Krijger RR; Wouters C; Wauters J; Oostra BA; Tibboel D; de Klein A
Am J Hum Genet; 2005 May; 76(5):877-82. PubMed ID: 15750894
[TBL] [Abstract][Full Text] [Related]
2. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.
Slavotinek AM; Moshrefi A; Davis R; Leeth E; Schaeffer GB; Burchard GE; Shaw GM; James B; Ptacek L; Pennacchio LA
Eur J Hum Genet; 2006 Sep; 14(9):999-1008. PubMed ID: 16736036
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia.
Scott DA; Klaassens M; Holder AM; Lally KP; Fernandes CJ; Galjaard RJ; Tibboel D; de Klein A; Lee B
Hum Mol Genet; 2007 Feb; 16(4):424-30. PubMed ID: 17210672
[TBL] [Abstract][Full Text] [Related]
4. Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature.
Klaassens M; Galjaard RJ; Scott DA; Brüggenwirth HT; van Opstal D; Fox MV; Higgins RR; Cohen-Overbeek TE; Schoonderwaldt EM; Lee B; Tibboel D; de Klein A
Am J Med Genet A; 2007 Sep; 143A(18):2204-12. PubMed ID: 17702015
[TBL] [Abstract][Full Text] [Related]
5. Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case.
Veredice C; Bianco F; Contaldo I; Orteschi D; Stefanini MC; Battaglia D; Lettori D; Guzzetta F; Zollino M
Epilepsia; 2009 Jul; 50(7):1810-5. PubMed ID: 19486360
[TBL] [Abstract][Full Text] [Related]
6. Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.
Kantarci S; Casavant D; Prada C; Russell M; Byrne J; Haug LW; Jennings R; Manning S; Boyd TK; Fryns JP; Holmes LB; Donahoe PK; Lee C; Kimonis V; Pober BR
Am J Med Genet A; 2006 Jan; 140(1):17-23. PubMed ID: 16333846
[TBL] [Abstract][Full Text] [Related]
7. Congenital diaphragmatic hernia associated with duplication of 11q23-qter.
Klaassens M; Scott DA; van Dooren M; Hochstenbach R; Eussen HJ; Cai WW; Galjaard RJ; Wouters C; Poot M; Laudy J; Lee B; Tibboel D; de Klein A
Am J Med Genet A; 2006 Jul; 140(14):1580-6. PubMed ID: 16770801
[TBL] [Abstract][Full Text] [Related]
8. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
Wat MJ; Shchelochkov OA; Holder AM; Breman AM; Dagli A; Bacino C; Scaglia F; Zori RT; Cheung SW; Scott DA; Kang SH
Am J Med Genet A; 2009 Aug; 149A(8):1661-77. PubMed ID: 19606479
[TBL] [Abstract][Full Text] [Related]
9. Congenital diaphragmatic hernia (CDH) etiology as revealed by pathway genetics.
Kantarci S; Donahoe PK
Am J Med Genet C Semin Med Genet; 2007 May; 145C(2):217-26. PubMed ID: 17436295
[TBL] [Abstract][Full Text] [Related]
10. Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia.
Wat MJ; Enciso VB; Wiszniewski W; Resnick T; Bader P; Roeder ER; Freedenberg D; Brown C; Stankiewicz P; Cheung SW; Scott DA
J Med Genet; 2010 Nov; 47(11):777-81. PubMed ID: 20921022
[TBL] [Abstract][Full Text] [Related]
11. Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
Wat MJ; Veenma D; Hogue J; Holder AM; Yu Z; Wat JJ; Hanchard N; Shchelochkov OA; Fernandes CJ; Johnson A; Lally KP; Slavotinek A; Danhaive O; Schaible T; Cheung SW; Rauen KA; Tonk VS; Tibboel D; de Klein A; Scott DA
J Med Genet; 2011 May; 48(5):299-307. PubMed ID: 21525063
[TBL] [Abstract][Full Text] [Related]
12. Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24).
Aviram-Goldring A; Daniely M; Frydman M; Shneyour Y; Cohen H; Barkai G
Am J Med Genet; 2000 Jan; 90(2):120-2. PubMed ID: 10607949
[TBL] [Abstract][Full Text] [Related]
13. Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
Slavotinek A; Lee SS; Davis R; Shrit A; Leppig KA; Rhim J; Jasnosz K; Albertson D; Pinkel D
J Med Genet; 2005 Sep; 42(9):730-6. PubMed ID: 16141010
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
López I; Bafalliu JA; Bernabé MC; García F; Costa M; Guillén-Navarro E
Prenat Diagn; 2006 Jun; 26(6):577-80. PubMed ID: 16700088
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
Hatem E; Meriam BR; Walid D; Adenen M; Moez G; Ali S
Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
[TBL] [Abstract][Full Text] [Related]
16. Congenital diaphragmatic hernia in Smith-Magenis syndrome: a possible locus at chromosome 17p11.2.
Sanford EF; Bermudez-Wagner K; Jeng LJ; Rauen KA; Slavotinek AM
Am J Med Genet A; 2011 Nov; 155A(11):2816-20. PubMed ID: 21965155
[TBL] [Abstract][Full Text] [Related]
17. Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development.
Schlembach D; Zenker M; Trautmann U; Ulmer R; Beinder E
Prenat Diagn; 2001 Apr; 21(4):289-92. PubMed ID: 11288119
[TBL] [Abstract][Full Text] [Related]
18. Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic hernia.
van Dooren MF; Brooks AS; Hoogeboom AJ; van den Hoonaard TL; de Klein JE; Wouters CH; Tibboel D
Am J Med Genet A; 2004 Jun; 127A(2):194-6. PubMed ID: 15108210
[TBL] [Abstract][Full Text] [Related]
19. A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
Arrington CB; Bleyl SB; Matsunami N; Bowles NE; Leppert TI; Demarest BL; Osborne K; Yoder BA; Byrne JL; Schiffman JD; Null DM; DiGeronimo R; Rollins M; Faix R; Comstock J; Camp NJ; Leppert MF; Yost HJ; Brunelli L
Am J Med Genet A; 2012 Dec; 158A(12):3137-47. PubMed ID: 23165927
[TBL] [Abstract][Full Text] [Related]
20. Congenital diaphragmatic hernia: is 15q26.1-26.2 a candidate locus?
Biggio JR; Descartes MD; Carroll AJ; Holt RL
Am J Med Genet A; 2004 Apr; 126A(2):183-5. PubMed ID: 15057983
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
