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 *

133 related articles for article (PubMed ID: 8957512)

  • 1. Zimmer phocomelia: delineation by principal coordinate analysis.
    Kosaki K; Jones MC; Stayboldt C
    Am J Med Genet; 1996 Dec; 66(1):55-9. PubMed ID: 8957512
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Roberts syndrome or "X-linked amelia"?
    Gershoni-Baruch R; Drugan A; Bronshtein M; Zimmer EZ
    Am J Med Genet; 1990 Dec; 37(4):569-72. PubMed ID: 2260610
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New autosomal recessive form of amelia.
    Michaud J; Filiatrault D; Dallaire L; Lambert M
    Am J Med Genet; 1995 Mar; 56(2):164-7. PubMed ID: 7625439
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome.
    Mollica F; Mazzone D; Cimino G; Opitz JM
    Am J Med Genet; 1995 Mar; 56(2):168-72. PubMed ID: 7625440
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tetra-phocomelia with multiple malformations: X-linked amelia, or Roberts syndrome, or DK-phocomelia syndrome?
    Rodríguez JI; Palacios J; Urioste M; Rodríguez-Peralto JL
    Am J Med Genet; 1992 Jun; 43(3):630-2. PubMed ID: 1605264
    [No Abstract]   [Full Text] [Related]  

  • 6. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA; Ismail S; Helmy NA
    Genet Couns; 2006; 17(1):1-13. PubMed ID: 16719272
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recurrent tetraamelia and pulmonary hypoplasia with multiple malformations in sibs.
    Rosenak D; Ariel I; Arnon J; Diamant YZ; Ben Chetrit A; Nadjari M; Zilberman R; Yaffe H; Cohen T; Ornoy A
    Am J Med Genet; 1991 Jan; 38(1):25-8. PubMed ID: 2012129
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Upper limb amelia, facial clefts, holoprosencephaly, and interrupted aortic arch.
    Zimpfer A; Miny P; Dombrowski U; Tolnay M; Meyer P; Bruder E
    Fetal Pediatr Pathol; 2007; 26(4):169-76. PubMed ID: 18075831
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of ectrodactyly and distal phocomelia.
    Delrue MA; Lacombe D
    Genet Couns; 2002; 13(3):319-25. PubMed ID: 12416640
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestations.
    Robins DB; Ladda RL; Thieme GA; Boal DK; Emanuel BS; Zackai EH
    Am J Med Genet; 1989 Mar; 32(3):390-4. PubMed ID: 2658590
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The importance of chromosome studies in Roberts syndrome/SC phocomelia and other cohesinopathies.
    Gerkes EH; van der Kevie-Kersemaekers AM; Yakin M; Smeets DF; van Ravenswaaij-Arts CM
    Eur J Med Genet; 2010; 53(1):40-4. PubMed ID: 19878742
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tetra-amelia and lung hypo/aplasia syndrome: new case report and review.
    Sousa SB; Pina R; Ramos L; Pereira N; Krahn M; Borozdin W; Kohlhase J; Amorim M; Gonnet K; Lévy N; Carreira IM; Couceiro AB; Saraiva JM
    Am J Med Genet A; 2008 Nov; 146A(21):2799-803. PubMed ID: 18837045
    [TBL] [Abstract][Full Text] [Related]  

  • 13. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.
    Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D
    Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DK-phocomelia syndrome in a child with a long follow-up.
    Urioste M; Paisán L; Martínez-Frías ML
    Am J Med Genet; 1994 Sep; 52(3):269-71. PubMed ID: 7810557
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection.
    Olney RS; Hoyme HE; Roche F; Ferguson K; Hintz S; Madan A
    Am J Med Genet; 2001 Nov; 103(4):295-301. PubMed ID: 11746009
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kyphomelic dysplasia: a report of a family with an autosomal dominant pattern.
    Toledo C; Navarro-Barros R; Alba L; Muñoz E
    Ann Genet; 1999; 42(3):170-3. PubMed ID: 10526661
    [TBL] [Abstract][Full Text] [Related]  

  • 17. von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.
    Lubinsky MS; Kahler SG; Speer IE; Hoyme HE; Kirillova IA; Lurie IW
    Am J Med Genet; 1994 Sep; 52(3):272-8. PubMed ID: 7810558
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tri-amelia and phocomelia with multiple malformations resembling Roberts syndrome in a fetus: is it a variant or a new syndrome?
    Song SY; Chi JG
    Clin Genet; 1996 Dec; 50(6):502-4. PubMed ID: 9147883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic findings in Roberts-SC phocomelia syndrome(s).
    Tomkins D; Hunter A; Roberts M
    Am J Med Genet; 1979; 4(1):17-26. PubMed ID: 495649
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D; Hadley DW; Tifft CJ; Biesecker LG
    Am J Med Genet; 2002 Jul; 110(4):308-14. PubMed ID: 12116202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.