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 *

193 related articles for article (PubMed ID: 10925390)

  • 1. Candidate region for Coffin-Siris syndrome at 7q32-->34.
    McGhee EM; Klump CJ; Bitts SM; Cotter PD; Lammer EJ
    Am J Med Genet; 2000 Jul; 93(3):241-3. PubMed ID: 10925390
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome.
    McPherson EW; Laneri G; Clemens MM; Kochmar SJ; Surti U
    Am J Med Genet; 1997 Sep; 71(4):430-3. PubMed ID: 9286450
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
    D'Alessandro E; Ligas C; Lo Re ML; Marcanio MP; Gentile T; Del Porto G
    J Med Genet; 1994 May; 31(5):413-5. PubMed ID: 8064823
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Duplication of C7orf58, WNT16 and FAM3C in an obese female with a t(7;22)(q32.1;q11.2) chromosomal translocation and clinical features resembling Coffin-Siris Syndrome.
    Zhu J; Qiu J; Magrane G; Abedalthagafi M; Zanko A; Golabi M; Chehab FF
    PLoS One; 2012; 7(12):e52353. PubMed ID: 23300646
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.
    Zweier C; Rittinger O; Bader I; Berland S; Cole T; Degenhardt F; Di Donato N; Graul-Neumann L; Hoyer J; Lynch SA; Vlasak I; Wieczorek D
    Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):290-301. PubMed ID: 25099957
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Numerous BAF complex genes are mutated in Coffin-Siris syndrome.
    Miyake N; Tsurusaki Y; Matsumoto N
    Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):257-61. PubMed ID: 25081545
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP; Kleczkowska A; van den Berghe H
    Clin Genet; 1988 Jan; 33(1):60-2. PubMed ID: 3342549
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Coffin-Siris syndrome.
    Schinzel A
    Acta Paediatr Scand; 1979 May; 68(3):449-52. PubMed ID: 155976
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variant of Coffin-Siris syndrome or previously undescribed syndrome?
    Braun-Quentin C; Kapferer L; Kotzot D
    Am J Med Genet; 1996 Sep; 64(4):568-72. PubMed ID: 8870924
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant syndrome resembling Coffin-Siris syndrome.
    Flynn MA; Milunsky JM
    Am J Med Genet A; 2006 Jun; 140(12):1326-30. PubMed ID: 16691594
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome.
    Vasileiou G; Vergarajauregui S; Endele S; Popp B; Büttner C; Ekici AB; Gerard M; Bramswig NC; Albrecht B; Clayton-Smith J; Morton J; Tomkins S; Low K; Weber A; Wenzel M; Altmüller J; Li Y; Wollnik B; Hoganson G; Plona MR; Cho MT; ; Thiel CT; Lüdecke HJ; Strom TM; Calpena E; Wilkie AOM; Wieczorek D; Engel FB; Reis A
    Am J Hum Genet; 2018 Mar; 102(3):468-479. PubMed ID: 29429572
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
    Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S
    Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Emergency cesarean in a patient with Coffin-Siris syndrome].
    Fornet I; Morillas P; López MA; Palacio FJ; Aguilar JM; Mesa JL
    Rev Esp Anestesiol Reanim; 2007 Nov; 54(9):563-5. PubMed ID: 18085110
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Coffin-Siris syndrome. Critical study of the literature apropos of a case].
    Foasso MF; Hermier M; Descos B; Collet JP; Perron F
    Pediatrie; 1983 Mar; 38(2):111-7. PubMed ID: 6622139
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome.
    Miyake N; Abdel-Salam G; Yamagata T; Eid MM; Osaka H; Okamoto N; Mohamed AM; Ikeda T; Afifi HH; Piard J; van Maldergem L; Mizuguchi T; Miyatake S; Tsurusaki Y; Matsumoto N
    Am J Med Genet A; 2016 Oct; 170(10):2662-70. PubMed ID: 27264538
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study.
    Fleck BJ; Pandya A; Vanner L; Kerkering K; Bodurtha J
    Am J Med Genet; 2001 Feb; 99(1):1-7. PubMed ID: 11170086
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Coffin-Siris syndrome in a 5-year-old girl].
    Meinecke P; Engelbrecht R; Schaefer E
    Monatsschr Kinderheilkd; 1986 Sep; 134(9):692-5. PubMed ID: 3785238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20.
    Vivarelli R; Zuffardi O; Maraschio P; Anichini C; Scarinci R
    Hum Genet; 1988 Aug; 79(4):385-8. PubMed ID: 3410463
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum.
    Coulibaly B; Sigaudy S; Girard N; Popovici C; Missirian C; Heckenroth H; Tasei AM; Fernandez C
    Eur J Med Genet; 2010; 53(5):318-21. PubMed ID: 20624500
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.