BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 20921022)

  • 1. 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]  

  • 2. Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci.
    Doelken SC; Seeger K; Hundsdoerfer P; Weber-Ferro W; Klopocki E; Graul-Neumann L
    Am J Med Genet A; 2013 Jan; 161A(1):218-24. PubMed ID: 23239641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions.
    Burgess T; Brown NJ; Stark Z; Bruno DL; Oertel R; Chong B; Calabro V; Kornberg A; Sanderson C; Kelly J; Howell KB; Savarirayan R; Hinds R; Greenway A; Slater HR; White SM
    Am J Med Genet A; 2014 Jan; 164A(1):77-86. PubMed ID: 24352913
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.
    Wat MJ; Beck TF; Hernández-García A; Yu Z; Veenma D; Garcia M; Holder AM; Wat JJ; Chen Y; Mohila CA; Lally KP; Dickinson M; Tibboel D; de Klein A; Lee B; Scott DA
    Hum Mol Genet; 2012 Sep; 21(18):4115-25. PubMed ID: 22723016
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital diaphragmatic hernia in WAGR syndrome.
    Scott DA; Cooper ML; Stankiewicz P; Patel A; Potocki L; Cheung SW
    Am J Med Genet A; 2005 May; 134(4):430-3. PubMed ID: 15779010
    [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. A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature.
    Chen Z; Chen H; Yuan K; Wang C
    BMC Med Genomics; 2020 Sep; 13(1):126. PubMed ID: 32894148
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. De novo copy number variants are associated with congenital diaphragmatic hernia.
    Yu L; Wynn J; Ma L; Guha S; Mychaliska GB; Crombleholme TM; Azarow KS; Lim FY; Chung DH; Potoka D; Warner BW; Bucher B; LeDuc CA; Costa K; Stolar C; Aspelund G; Arkovitz MS; Chung WK
    J Med Genet; 2012 Oct; 49(10):650-9. PubMed ID: 23054247
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects.
    Keitges EA; Pasion R; Burnside RD; Mason C; Gonzalez-Ruiz A; Dunn T; Masiello M; Gebbia JA; Fernandez CO; Risheg H
    Am J Med Genet A; 2013 Jul; 161A(7):1755-8. PubMed ID: 23696316
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital diaphragmatic hernia is part of the new 15q24 microdeletion syndrome.
    Van Esch H; Backx L; Pijkels E; Fryns JP
    Eur J Med Genet; 2009; 52(2-3):153-6. PubMed ID: 19233321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP; Wang YL; Chern SR; Liu YP; Peng CR; Kuo YL; Wu PS; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disorders of sex development and Diamond-Blackfan anemia: is there an association?
    Hoefele J; Bertrand AM; Stehr M; Leblanc T; Tchernia G; Simansour M; Mignot B; Alberer M; Schwarz HP; Da Costa L;
    Pediatr Nephrol; 2010 Jul; 25(7):1255-61. PubMed ID: 20358230
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.