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 *

143 related articles for article (PubMed ID: 16835920)

  • 1. Paternal isodisomy of chromosome 7 with cystic fibrosis and overgrowth.
    Fares F; David M; Lerner A; Diukman R; Lerer I; Abeliovich D; Rivlin J
    Am J Med Genet A; 2006 Aug; 140(16):1785-8. PubMed ID: 16835920
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case of paternal uniparental isodisomy for chromosome 7 associated with overgrowth.
    Nakamura A; Muroya K; Ogata-Kawata H; Nakabayashi K; Matsubara K; Ogata T; Kurosawa K; Fukami M; Kagami M
    J Med Genet; 2018 Aug; 55(8):567-570. PubMed ID: 29455159
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: a new patient presenting with normal growth.
    Le Caignec C; Isidor B; de Pontbriand U; David V; Audrezet MP; Ferec C; David A
    Am J Med Genet A; 2007 Nov; 143A(22):2696-9. PubMed ID: 17935233
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?
    Voss R; Ben-Simon E; Avital A; Godfrey S; Zlotogora J; Dagan J; Tikochinski Y; Hillel J
    Am J Hum Genet; 1989 Sep; 45(3):373-80. PubMed ID: 2570528
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders.
    Xiao P; Liu P; Weber JL; Papasian CJ; Recker RR; Deng HW
    Hum Mutat; 2006 Feb; 27(2):133-7. PubMed ID: 16429396
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cystic fibrosis and Russell-Silver syndrome in a child with maternal isodisomy of chromosome 7.
    Sonnappa S; Prescott K; Adler B; Dinwiddie R; Wallis C
    Pediatr Pulmonol; 2005 Aug; 40(2):166-8. PubMed ID: 15965898
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.
    Kotzot D; Schmitt S; Bernasconi F; Robinson WP; Lurie IW; Ilyina H; Méhes K; Hamel BC; Otten BJ; Hergersberg M
    Hum Mol Genet; 1995 Apr; 4(4):583-7. PubMed ID: 7633407
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaic maternal uniparental isodisomy for chromosome 7q21-qter.
    Reboul MP; Tandonnet O; Biteau N; Belet-de Putter C; Rebouissoux L; Moradkhani K; Vu PY; Saura R; Arveiler B; Lacombe D; Taine L; Iron A
    Clin Genet; 2006 Sep; 70(3):207-13. PubMed ID: 16922723
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause.
    Hannula K; Lipsanen-Nyman M; Kristo P; Kaitila I; Simola KO; Lenko HL; Tapanainen P; Holmberg C; Kere J
    Pediatrics; 2002 Mar; 109(3):441-8. PubMed ID: 11875139
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum features.
    Berland S; Rustad CF; Bentsen MHL; Wollen EJ; Turowski G; Johansson S; Houge G; Haukanes BI
    Cold Spring Harb Mol Case Stud; 2021 Dec; 7(6):. PubMed ID: 34615670
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7.
    Giardina E; Peconi C; Cascella R; Sinibaldi C; Foti Cuzzola V; Nardone AM; Bramanti P; Novelli G
    Electrophoresis; 2009 Jun; 30(11):2008-11. PubMed ID: 19517448
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mosaic paternal genome-wide uniparental isodisomy with down syndrome.
    Darcy D; Atwal PS; Angell C; Gadi I; Wallerstein R
    Am J Med Genet A; 2015 Oct; 167A(10):2463-9. PubMed ID: 26219535
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
    Slatter RE; Elliott M; Welham K; Carrera M; Schofield PN; Barton DE; Maher ER
    J Med Genet; 1994 Oct; 31(10):749-53. PubMed ID: 7837249
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Uniparental disomy as a mechanism for human genetic disease.
    Spence JE; Perciaccante RG; Greig GM; Willard HF; Ledbetter DH; Hejtmancik JF; Pollack MS; O'Brien WE; Beaudet AL
    Am J Hum Genet; 1988 Feb; 42(2):217-26. PubMed ID: 2893543
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paternal uniparental disomy of chromosome 14: confirmation of a clinically-recognizable phenotype.
    Stevenson DA; Brothman AR; Chen Z; Bayrak-Toydemir P; Longo N
    Am J Med Genet A; 2004 Sep; 130A(1):88-91. PubMed ID: 15368501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Growth parameters in maternal uniparental disomy 7 and 14.
    Kotzot D
    Eur J Pediatr; 2007 Nov; 166(11):1143-9. PubMed ID: 17203278
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of segmental paternal isodisomy of chromosome 14.
    Coveler KJ; Yang SP; Sutton R; Milstein JM; Wu YQ; Bois KD; Beischel LS; Johnson JP; Shaffer LG
    Hum Genet; 2002 Mar; 110(3):251-6. PubMed ID: 11935337
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.
    Höglund P; Holmberg C; de la Chapelle A; Kere J
    Am J Hum Genet; 1994 Oct; 55(4):747-52. PubMed ID: 7942853
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Uniparental disomy: a review of causes and clinical sequelae].
    Engel E
    Ann Genet; 1995; 38(3):113-36. PubMed ID: 8540683
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.
    Hosoki K; Ogata T; Kagami M; Tanaka T; Saitoh S
    Eur J Hum Genet; 2008 Aug; 16(8):1019-23. PubMed ID: 18478039
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.