These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 22847911)

  • 21. 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]  

  • 22. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: a new case and discussion of the literature.
    Hengstschläger M; Mittermayer C; Repa C; Drahonsky R; Deutinger J; Bernaschek G
    Fetal Diagn Ther; 2004; 19(6):510-2. PubMed ID: 15539876
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.
    Qi Z; Jeng LJ; Slavotinek A; Yu J
    BMC Med Genomics; 2015 Jul; 8():38. PubMed ID: 26174853
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur.
    Abdelhedi F; Corcos J; Cuisset L; Tsatsaris V; Tantau J; Le Tessier D; Lebbar A; Dupont JM
    Am J Med Genet A; 2012 Mar; 158A(3):617-21. PubMed ID: 22302515
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.
    Shaffer LG; Theisen A; Bejjani BA; Ballif BC; Aylsworth AS; Lim C; McDonald M; Ellison JW; Kostiner D; Saitta S; Shaikh T
    Genet Med; 2007 Sep; 9(9):607-16. PubMed ID: 17873649
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.
    Quélin C; Bendavid C; Dubourg C; de la Rochebrochard C; Lucas J; Henry C; Jaillard S; Loget P; Loeuillet L; Lacombe D; Rival JM; David V; Odent S; Pasquier L
    Eur J Med Genet; 2009; 52(1):41-6. PubMed ID: 19022413
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Duplication of the ZIC2 gene is not associated with holoprosencephaly.
    Jobanputra V; Burke A; Kwame AY; Shanmugham A; Shirazi M; Brown S; Warburton PE; Levy B; Warburton D
    Am J Med Genet A; 2012 Jan; 158A(1):103-8. PubMed ID: 22105922
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.
    Yang YF; Ai Q; Huang C; Chen JL; Wang J; Xie L; Zhang WZ; Yang JF; Tan ZP
    Gene; 2013 Oct; 528(1):51-4. PubMed ID: 23639964
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1q.
    Bartsch C; Aslan M; Köhler J; Miny P; Horst J; Holzgreve W; Rehder H; Fritz B
    Fetal Diagn Ther; 2001; 16(5):265-73. PubMed ID: 11509847
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tissue-specific mosaicism among fetuses with prenatally diagnosed diaphragmatic hernia.
    Donnenfeld AE; Campbell TJ; Byers J; Librizzi RJ; Weiner S
    Am J Obstet Gynecol; 1993 Oct; 169(4):1017-21. PubMed ID: 8238112
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences.
    Marlet L; Alix E; Till M; Raskin-Champion F; Attia J; Boggio D; Sanlaville D; Schluth-Bolard C
    Cytogenet Genome Res; 2017; 153(3):117-124. PubMed ID: 29268249
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.