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 *

89 related articles for article (PubMed ID: 11494967)

  • 1. Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition.
    Martin DM; Gorski JL
    J Med Genet; 2001 Aug; 38(8):547-51. PubMed ID: 11494967
    [No Abstract]   [Full Text] [Related]  

  • 2. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
    Guttmacher AE
    Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hypoplastic left heart and postaxial polydactyly.
    Brennan P
    Clin Dysmorphol; 2001 Jul; 10(3):219-22. PubMed ID: 11446418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A postaxial polydactyly and progressive myopia syndrome of autosomal dominant origin.
    Czeizel A; Brooser G
    Clin Genet; 1986 Nov; 30(5):406-8. PubMed ID: 3802559
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance.
    Faivre L; Le Merrer M; Baumann C; Polak M; Chatelain P; Sulmont V; Cousin J; Bost M; Cordier MP; Zackai E; Russell K; Finidori G; Pouliquen JC; Munnich A; Maroteaux P; Cormier-Daire V
    J Med Genet; 2001 Nov; 38(11):745-9. PubMed ID: 11694546
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hirschsprung disease, postaxial polydactyly, and atrial septal defect.
    Nowaczyk MJ; James AG; Superina R; Siegel-Bartelt J
    Am J Med Genet; 1997 Jan; 68(1):74-5. PubMed ID: 8986280
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An Indian family with postaxial polydactyly in four generations.
    Kucheria K; Kenue RK; Taneja N
    Clin Genet; 1981 Jul; 20(1):36-9. PubMed ID: 7296946
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Congenital cardiopathies and associated bone abnormalities].
    Pigeon Oliveros H; Pérez Treviño C; Rodríguez García I
    Bol Med Hosp Infant Mex; 1979; 36(1):135-47. PubMed ID: 214095
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?
    Kwee ML; Lindhout D
    Clin Genet; 1983 Sep; 24(3):200-5. PubMed ID: 6627724
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Scalp defects, polythelia, microcephaly, and developmental delay: a new syndrome with apparent autosomal dominant inheritance.
    Marble M; Pridjian G
    Am J Med Genet; 2002 Apr; 108(4):327-32. PubMed ID: 11920840
    [TBL] [Abstract][Full Text] [Related]  

  • 11. B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?
    Edery P; Le Deist F; Briard ML; Debré M; Munnich A; Griscelli C; Fischer A; Lyonnet S
    J Med Genet; 2001 Jul; 38(7):488-93. PubMed ID: 11476068
    [No Abstract]   [Full Text] [Related]  

  • 12. [Giant-cell retinal dysplasia in microphthalmos].
    Mocanu C; Simionescu C
    Oftalmologia; 1994; 38(4):348-54. PubMed ID: 7947673
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.
    Fried K; Liban E; Lurie M; Friedman S; Reisner SH
    J Med Genet; 1971 Sep; 8(3):285-90. PubMed ID: 4999589
    [No Abstract]   [Full Text] [Related]  

  • 14. Child with overgrowth, pigmentary streaks, polydactyly, and intestinal lymphangiectasia: macrocephaly-cutis marmorata telangiectatica congenita syndrome or new disorder?
    Mégarbané A; Haddad J; Lyonnet S; Clayton-Smith J
    Am J Med Genet A; 2003 Jan; 116A(2):184-7. PubMed ID: 12494441
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.
    Halal F; Homsy M; Perreault G
    Am J Med Genet; 1984 Apr; 17(4):753-62. PubMed ID: 6426304
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype.
    Tekin M; Kavaz A; Berberoğlu M; Fitoz S; Ekim M; Ocal G; Akar N
    Am J Med Genet A; 2004 Oct; 130A(3):284-7. PubMed ID: 15378538
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Postaxial polydactyly, ulnar ray dysgenesis, and renal cystic dysplasia in sibs.
    Kaplan BS; Bellah RD
    Am J Med Genet; 1999 Dec; 87(5):426-9. PubMed ID: 10594882
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absent tibiae--polydactyly--triphalangeal thumbs with fibular dimelia: variable expression of the Werner (McKusick 188770) syndrome?
    Vargas FR; Pontes RL; Llerena Júnior JC; de Almeida JC
    Am J Med Genet; 1995 Jan; 55(3):261-4. PubMed ID: 7726219
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3.
    Brickwood S; Bonthron DT; Al-Gazali LI; Piper K; Hearn T; Wilson DI; Hanley NA
    J Med Genet; 2003 Sep; 40(9):685-9. PubMed ID: 12960215
    [No Abstract]   [Full Text] [Related]  

  • 20. Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
    Debeer P; Van Esch H; Huysmans C; Pijkels E; De Smet L; Van de Ven W; Devriendt K; Fryns JP
    Eur J Med Genet; 2005; 48(4):377-87. PubMed ID: 16378922
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.