BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 3605217)

  • 1. Radial ray defect and Duane anomaly: report of a family with autosomal dominant transmission.
    MacDermot KD; Winter RM
    Am J Med Genet; 1987 Jun; 27(2):313-9. PubMed ID: 3605217
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalities.
    Hurst JA; Baraitser M; Wonke B
    Am J Med Genet; 1991 Sep; 40(4):482-4. PubMed ID: 1746615
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An autosomal dominant syndrome of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.
    Schmitt E; Gillenwater JY; Kelly TE
    Am J Med Genet; 1982 Sep; 13(1):63-9. PubMed ID: 7137222
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. The Okihiro syndrome of Duane anomaly, radial ray abnormalities, and deafness.
    Hayes A; Costa T; Polomeno RC
    Am J Med Genet; 1985 Oct; 22(2):273-80. PubMed ID: 4050857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generations.
    Collins A; Baraitser M; Pembrey M
    Clin Dysmorphol; 1993 Jul; 2(3):237-40. PubMed ID: 8287186
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New autosomal dominant radial ray hypoplasia syndrome.
    Goldblatt J; Viljoen D
    Am J Med Genet; 1987 Nov; 28(3):647-54. PubMed ID: 3425633
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?
    Stoll C; Alembik Y; Dott B
    Ann Genet; 1994; 37(4):207-9. PubMed ID: 7710257
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome.
    Pelias MZ; Superneau DW; Thurmon TF
    Am J Med Genet; 1981; 10(2):133-9. PubMed ID: 7315870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.
    Galjaard RJ; Kostakoglu N; Hoogeboom JJ; Breedveld GJ; van der Linde HC; Hovius SE; Oostra BA; Sandkuijl LA; Akarsu AN; Heutink P
    Eur J Hum Genet; 2001 Sep; 9(9):653-8. PubMed ID: 11571552
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dominant inheritance of a syndrome similar to Rubinstein-Taybi.
    Cotsirilos P; Taylor JC; Matalon R
    Am J Med Genet; 1987 Jan; 26(1):85-93. PubMed ID: 3812583
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Radial ray aplasia and renal anomalies in father and son: a new syndrome.
    Sofer S; Bar-Ziv J; Abeliovich D
    Am J Med Genet; 1983 Jan; 14(1):151-7. PubMed ID: 6829604
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformations.
    Kurnit DM; Steele MW; Pinsky L; Dibbins A
    J Pediatr; 1978 Aug; 93(2):270-3. PubMed ID: 671168
    [No Abstract]   [Full Text] [Related]  

  • 14. Further delineation of the Baller-Gerold syndrome.
    Lin AE; McPherson E; Nwokoro NA; Clemens M; Losken HW; Mulvihill JJ
    Am J Med Genet; 1993 Feb; 45(4):519-24. PubMed ID: 8465861
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22.
    Cullen P; Rodgers CS; Callen DF; Connolly VM; Eyre H; Fells P; Gordon H; Winter RM; Thakker RV
    Am J Med Genet; 1993 Nov; 47(6):925-30. PubMed ID: 8279492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Further delineation of the acro-renal-ocular syndrome.
    Aalfs CM; van Schooneveld MJ; van Keulen EM; Hennekam RC
    Am J Med Genet; 1996 Mar; 62(3):276-81. PubMed ID: 8882787
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hypoplasia of the tibia, polydactyly, and triphalangeal thumb: 1st family described in Venezuela].
    Martínez-Basalo C; González-Inciarte ME; Delgado-Luengo W; Casilla-Nava S; González-Incíarte L; Alvarez-Nava F; Boscán-Porras N; Delgado-Luengo J
    Invest Clin; 1997 Dec; 38(4):219-26. PubMed ID: 9527389
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders.
    Kohlhase J; Chitayat D; Kotzot D; Ceylaner S; Froster UG; Fuchs S; Montgomery T; Rösler B
    Hum Mutat; 2005 Sep; 26(3):176-83. PubMed ID: 16086360
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.