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 *

268 related articles for article (PubMed ID: 24878679)

  • 21. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
    Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
    Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesis.
    Thorwarth A; Mueller I; Biebermann H; Ropers HH; Grueters A; Krude H; Ullmann R
    J Clin Endocrinol Metab; 2010 Jul; 95(7):3446-52. PubMed ID: 20427504
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic Analyses in Small-for-Gestational-Age Newborns.
    Stalman SE; Solanky N; Ishida M; Alemán-Charlet C; Abu-Amero S; Alders M; Alvizi L; Baird W; Demetriou C; Henneman P; James C; Knegt LC; Leon LJ; Mannens MMAM; Mul AN; Nibbering NA; Peskett E; Rezwan FI; Ris-Stalpers C; van der Post JAM; Kamp GA; Plötz FB; Wit JM; Stanier P; Moore GE; Hennekam RC
    J Clin Endocrinol Metab; 2018 Mar; 103(3):917-925. PubMed ID: 29342293
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Analysis copy number variation of Chinese children in early-onset epileptic encephalopathies with unknown cause.
    Ma Y; Chen C; Wang Y; Wu L; He F; Chen C; Zhang C; Deng X; Yang L; Chen Y; Wu L; Yin F; Peng J
    Clin Genet; 2016 Nov; 90(5):428-436. PubMed ID: 26925868
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Two short children born small for gestational age with insulin-like growth factor 1 receptor haploinsufficiency illustrate the heterogeneity of its phenotype.
    Ester WA; van Duyvenvoorde HA; de Wit CC; Broekman AJ; Ruivenkamp CA; Govaerts LC; Wit JM; Hokken-Koelega AC; Losekoot M
    J Clin Endocrinol Metab; 2009 Dec; 94(12):4717-27. PubMed ID: 19864454
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Array CGH analysis of a cohort of Russian patients with intellectual disability.
    Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN
    Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A de novo microtriplication at 4q21.21-q21.22 in a patient with a vascular malignant hemangioma, elongated sigmoid colon, developmental delay, and absence of speech.
    Lebedev IN; Nazarenko LP; Skryabin NA; Babushkina NP; Kashevarova AA
    Am J Med Genet A; 2016 Aug; 170(8):2089-96. PubMed ID: 27288323
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].
    He WZ; Liu WQ; Zhong XQ; Chen XL; Li SY; Zhang HM; Li Q; Cui QL; Sun XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun; 29(3):266-9. PubMed ID: 22678785
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
    Derwińska K; Bartnik M; Wiśniowiecka-Kowalnik B; Jagła M; Rudziński A; Pietrzyk JJ; Kawalec W; Ziółkowska L; Kutkowska-Kaźmierczak A; Gambin T; Sykulski M; Shaw CA; Gambin A; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
    Med Wieku Rozwoj; 2012; 16(3):175-82. PubMed ID: 23378395
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
    Warburton D; Ronemus M; Kline J; Jobanputra V; Williams I; Anyane-Yeboa K; Chung W; Yu L; Wong N; Awad D; Yu CY; Leotta A; Kendall J; Yamrom B; Lee YH; Wigler M; Levy D
    Hum Genet; 2014 Jan; 133(1):11-27. PubMed ID: 23979609
    [TBL] [Abstract][Full Text] [Related]  

  • 31. High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease.
    Zhao W; Niu G; Shen B; Zheng Y; Gong F; Wang X; Lee J; Mulvihill JJ; Chen X; Li S
    Am J Med Genet A; 2013 Dec; 161A(12):3087-94. PubMed ID: 24115576
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.
    Fry AE; Rees E; Thompson R; Mantripragada K; Blake P; Jones G; Morgan S; Jose S; Mugalaasi H; Archer H; McCann E; Clarke A; Taylor C; Davies S; Gibbon F; Te Water Naude J; Hartley L; Thomas G; White C; Natarajan J; Thomas RH; Drew C; Chung SK; Rees MI; Holmans P; Owen MJ; Kirov G; Pilz DT; Kerr MP
    BMC Med Genet; 2016 Apr; 17(1):34. PubMed ID: 27113213
    [TBL] [Abstract][Full Text] [Related]  

  • 33. De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.
    Yu Y; Yao R; Wang L; Fan Y; Huang X; Hirschhorn J; Dauber A; Shen Y
    BMC Genomics; 2015 Sep; 16(1):701. PubMed ID: 26376624
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
    Bartnik M; Szczepanik E; Derwińska K; Wiśniowiecka-Kowalnik B; Gambin T; Sykulski M; Ziemkiewicz K; Kędzior M; Gos M; Hoffman-Zacharska D; Mazurczak T; Jeziorek A; Antczak-Marach D; Rudzka-Dybała M; Mazurkiewicz H; Goszczańska-Ciuchta A; Zalewska-Miszkurka Z; Terczyńska I; Sobierajewicz M; Shaw CA; Gambin A; Mierzewska H; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
    Am J Med Genet B Neuropsychiatr Genet; 2012 Oct; 159B(7):760-71. PubMed ID: 22825934
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Infantile spasms are associated with abnormal copy number variations.
    Tiwari VN; Sundaram SK; Chugani HT; Huq AH
    J Child Neurol; 2013 Oct; 28(10):1191-6. PubMed ID: 22914377
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of novel candidate disease genes from de novo exonic copy number variants.
    Gambin T; Yuan B; Bi W; Liu P; Rosenfeld JA; Coban-Akdemir Z; Pursley AN; Nagamani SCS; Marom R; Golla S; Dengle L; Petrie HG; Matalon R; Emrick L; Proud MB; Treadwell-Deering D; Chao HT; Koillinen H; Brown C; Urraca N; Mostafavi R; Bernes S; Roeder ER; Nugent KM; Bader PI; Bellus G; Cummings M; Northrup H; Ashfaq M; Westman R; Wildin R; Beck AE; Immken L; Elton L; Varghese S; Buchanan E; Faivre L; Lefebvre M; Schaaf CP; Walkiewicz M; Yang Y; Kang SL; Lalani SR; Bacino CA; Beaudet AL; Breman AM; Smith JL; Cheung SW; Lupski JR; Patel A; Shaw CA; Stankiewicz P
    Genome Med; 2017 Sep; 9(1):83. PubMed ID: 28934986
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Clinical phenotypes and copy number variations in children with microdeletion and microduplication syndromes: an analysis of 50 cases].
    Zhang LN; Meng Z; He ZW; Li DF; Luo XY; Liang LY
    Zhongguo Dang Dai Er Ke Za Zhi; 2016 Sep; 18(9):840-845. PubMed ID: 27655541
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Copy number variants in adult patients with Lennox-Gastaut syndrome features.
    Lund C; Brodtkorb E; Røsby O; Rødningen OK; Selmer KK
    Epilepsy Res; 2013 Jul; 105(1-2):110-7. PubMed ID: 23415449
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Clinical features and genome-wide copy number variation analysis in 60 children with early-onset epileptic encephalopathies of unknown cause].
    Ma YP; Peng J; Wang Y; Chen Y; Wu LW; Yin F
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Nov; 16(11):1100-4. PubMed ID: 25406551
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.