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 *

207 related articles for article (PubMed ID: 9401100)

  • 1. Floating Harbor syndrome. Case report and further syndrome delineation.
    Midro AT; Olchowik B; Rogowska M; Hubert E; Hassman-Poznańska E; Papasz A; Szulc S; Wiśniewski A
    Ann Genet; 1997; 40(3):133-8. PubMed ID: 9401100
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Changing phenotype in Floating-Harbor syndrome.
    Hersh JH; Groom KR; Yen FF; Verdi GD
    Am J Med Genet; 1998 Feb; 76(1):58-61. PubMed ID: 9508066
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Floating-Harbor syndrome. A neuropsychological approach.
    Davalos IP; Figuera LE; Bobadilla L; Martinez-Martinez R; Matute E; Partida MG; Bañuelos LA; Ramirez-Dueñas ML
    Genet Couns; 1996; 7(4):283-8. PubMed ID: 8985732
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A; Seven M; Deviren A; Söylemez MA; Hacihanefioğlu S; Ulutin T; Cenani A
    Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndrome.
    Doerfler W; Wieczorek D; Gillessen-Kaesbach G; Albrecht B; Passarge E
    Am J Med Genet; 1997 Dec; 73(2):210-6. PubMed ID: 9409875
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndrome.
    Smeets E; Fryns JP; Van den Berghe H
    Genet Couns; 1996; 7(2):143-6. PubMed ID: 8831134
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Floating-Harbor syndrome in a girl with somatic asymmetry].
    Midro AT; Rogowska M; Hubert E; Hassman-Poznańska E; Popko J
    Pediatr Pol; 1995 Sep; 70(9):775-8. PubMed ID: 8657512
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Weaver syndrome in two Japanese children.
    Kondo I; Mori Y; Kuwajima K
    Am J Med Genet; 1991 Nov; 41(2):221-4. PubMed ID: 1785638
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutchinick syndrome in a Japanese girl.
    Tonoki H; Hattori T; Kamoshida H; Ohta Y; Niikawa N
    Am J Med Genet; 1999 Mar; 83(2):96-9. PubMed ID: 10190479
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L; El-Nabi MM; Azab AS; Gouda SA; Al-Wadaani AM; Naguib KK
    East Mediterr Health J; 2007; 13(4):975-9. PubMed ID: 17955782
    [No Abstract]   [Full Text] [Related]  

  • 11. Niikawa-Kuroki syndrome.
    Roccella M
    Minerva Pediatr; 1999; 51(7-8):271-8. PubMed ID: 10634060
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Floating-Harbor syndrome: case report.
    Genc G; Sarac A; Erkek Atay N; Kulali F
    Minerva Pediatr; 2008 Apr; 60(2):249-51. PubMed ID: 18449141
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V; Rozsnyai K; Farcaş S; Velea I; Fryns JP
    Genet Couns; 2005; 16(2):167-71. PubMed ID: 16080297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Delineation of the da-Silva syndrome.
    Naritomi K; Tohma T; Goya Y; Shiroma N; Hirayama K
    Am J Med Genet; 1994 Feb; 49(3):313-6. PubMed ID: 8209892
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Not all floating-harbor syndrome cases are due to mutations in exon 34 of SRCAP.
    Le Goff C; Mahaut C; Bottani A; Doray B; Goldenberg A; Moncla A; Odent S; Nitschke P; Munnich A; Faivre L; Cormier-Daire V
    Hum Mutat; 2013 Jan; 34(1):88-92. PubMed ID: 22965468
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype].
    Blanco-Barca O; Gallego-Blanco M; Ruiz-Ponte C; Barros-Angueira F; Esquete-López C; Eirís-Puñal J; Castro-Gago M
    Rev Neurol; 2004 Jun 1-15; 38(11):1038-42. PubMed ID: 15202082
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and genetic characteristics and effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome.
    García RJ; Kant SG; Wit JM; Mericq V
    J Pediatr Endocrinol Metab; 2012; 25(1-2):207-12. PubMed ID: 22570979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
    Mégarbané A; Abi Moussa M
    Genet Couns; 1997; 8(2):127-32. PubMed ID: 9219011
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A variant example of familial Floating-Harbor syndrome?
    Peñaloza JM; García-Cruz D; Dávalos IP; Dávalos NO; García-Cruz MO; Pérez-Rulfo D; Sánchez-Corona J
    Genet Couns; 2003; 14(1):31-7. PubMed ID: 12725587
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.