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 *

169 related articles for article (PubMed ID: 11045592)

  • 1. Amniotic band sequence versus the autosomal recessive microcephaly, facial clefting, and preaxial polydactyly syndrome.
    Guion-Almeida ML; Richieri-Costa A
    Clin Dysmorphol; 2000 Oct; 9(4):297-9. PubMed ID: 11045592
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three cases of oblique facial cleft.
    Mishima K; Sugahara T; Mori Y; Sakuda M
    J Craniomaxillofac Surg; 1996 Dec; 24(6):372-7. PubMed ID: 9032606
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clefting, amniotic bands, and polydactyly: a distinct phenotype that supports an intrinsic mechanism for amniotic band sequence.
    Robin NH; Franklin J; Prucka S; Ryan AB; Grant JH
    Am J Med Genet A; 2005 Sep; 137A(3):298-301. PubMed ID: 16088913
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Another case of microcephaly, facial clefting, and preaxial polydactyly.
    Marles SL; Chudley AE
    J Med Genet; 1990 Sep; 27(9):593-4. PubMed ID: 2231655
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia.
    Verloes A; Dresse MF; Keutgen H; Asplund C; Smith CI
    Am J Med Genet; 2001 Jul; 101(3):209-12. PubMed ID: 11424135
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Preaxial polydactyly in an individual with Wiedemann-Steiner syndrome caused by a novel nonsense mutation in KMT2A.
    Enokizono T; Ohto T; Tanaka R; Tanaka M; Suzuki H; Sakai A; Imagawa K; Fukushima H; Iwabuti A; Fukushima T; Sumazaki R; Uehara T; Takenouchi T; Kosaki K
    Am J Med Genet A; 2017 Oct; 173(10):2821-2825. PubMed ID: 28815892
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Amniotic band syndrome and a 47, XYY karyotype].
    Hernando I; Plasencia A; Peña E; Fernández Pérez M; Benavides A; Rodríguez de la Rúa MV; Fernández Toral J
    An Esp Pediatr; 1987 Jul; 27(1):75-6. PubMed ID: 3662260
    [No Abstract]   [Full Text] [Related]  

  • 8. Typical facial clefting and constriction band anomalies: an unusual association in three unrelated patients.
    Taub PJ; Bradley JP; Setoguchi Y; Schimmenti L; Kawamoto HK
    Am J Med Genet A; 2003 Jul; 120A(2):256-60. PubMed ID: 12833410
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. A new case of holoprosencephaly-polydactyly syndrome with alobar holoprosencephaly, preaxial polydactyly and congenital glaucoma.
    Sandal G; Tok L; Ormeci AR
    Genet Couns; 2014; 25(1):49-52. PubMed ID: 24783655
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unknown syndrome: microcephaly, facial clefting, and preaxial polydactyly.
    Howard FM; Young ID
    J Med Genet; 1988 Apr; 25(4):272-3. PubMed ID: 3367355
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An infant with large fontanelles, aplasia cutis congenita, tessier facial cleft, polydactyly inversus, and toe syndactyly: a previously undescribed syndrome?
    Jackson J; Delk P; Farrow E; Griffith C; Lah M; Weaver DD
    Am J Med Genet A; 2015 Apr; 167A(4):683-7. PubMed ID: 25708102
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Midline Cleft of Lip With Preaxial Polydactyly in One Hand: A Possible New Variation of Thurston Syndrome?
    Jain K; Singh M
    Cleft Palate Craniofac J; 2020 Apr; 57(4):524-528. PubMed ID: 31648526
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Documentation of anomalies not previously described in Fryns syndrome.
    Arnold SR; Debich-Spicer D D; Opitz JM; Gilbert-Barness E
    Am J Med Genet A; 2003 Jan; 116A(2):179-82; discussion 183. PubMed ID: 12494439
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Femoral facial syndrome with bilateral agenesis of femora and preaxial polydactyly of the feet in a Chinese stillborn.
    Poon WL; Yuen MK; Ng SK; Leung YM
    Clin Imaging; 2006; 30(5):357-60. PubMed ID: 16919561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Roentgenologic features of the Meckel syndrome.
    Seppänen U; Herva R
    Pediatr Radiol; 1983; 13(6):329-31. PubMed ID: 6646886
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders.
    Colombani M; Laurent N; Le Merrer M; Delezoide AL; Thauvin-Robinet C; Huet F; Sagot P; Couvreur S; Rousseau T; Robertson SP; Faivre L
    Prenat Diagn; 2006 Dec; 26(12):1151-5. PubMed ID: 17009344
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes.
    Dincsoy MY; Salih MA; al-Jurayyan N; al Saadi M; Patel PJ
    Am J Med Genet; 1995 Apr; 56(3):317-21. PubMed ID: 7778599
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Amniotic bands and the EEC syndrome.
    Guion-Almeida ML; Rodini ES; Pereira SC; Richieri-Costa A
    Birth Defects Orig Artic Ser; 1996; 30(1):171-7. PubMed ID: 9125326
    [No Abstract]   [Full Text] [Related]  

  • 20. Picture of the month. Amniotic constriction bands (Streeter dysplasia, ring constrictions).
    Feingold M
    Am J Dis Child; 1984 Feb; 138(2):199-200. PubMed ID: 6695880
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.