BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 8957515)

  • 21. Pseudo-trisomy 13 syndrome.
    Cohen MM; Gorlin RJ
    Am J Med Genet; 1991 Jun; 39(3):332-5; discussion 336-7. PubMed ID: 1867286
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A review of 35 cases of asymmetric crying facies.
    Caksen H; Odabaş D; Tuncer O; Kirimi E; Tombul T; Ikbal M; Ataş B; Ari Yuca S
    Genet Couns; 2004; 15(2):159-65. PubMed ID: 15287415
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs.
    Urioste M; Arroyo A; Martínez-Frías ML
    Am J Med Genet; 1991 Dec; 41(4):475-7. PubMed ID: 1776641
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
    Saal HM; Greenstein RM; Weinbaum PJ; Poole AE
    Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The CHARGE association in a newborn infant.
    Akisü M; Ozkinay F; Ozyürek R; Küçüktaş A; Kültürsay N
    Turk J Pediatr; 1998; 40(2):283-7. PubMed ID: 9714686
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM; Winter RM
    Am J Med Genet; 1988 Jul; 30(3):719-24. PubMed ID: 3055984
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Unusual association of congenital malformations: craniosynostosis, heart defect, abnormal intestinal innervation and urogenital abnormalities.
    Van Nesselrooij BP; Spliet W; Beemer FA
    Clin Dysmorphol; 1998 Jan; 7(1):51-3. PubMed ID: 9546831
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Autosomal recessive syndrome of sacral and conotruncal developmental field defects (Kousseff syndrome).
    Toriello HV; Sharda JK; Beaumont EJ
    Am J Med Genet; 1985 Oct; 22(2):357-60. PubMed ID: 4050868
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
    Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
    Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Filippi syndrome: report of three additional cases.
    Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
    Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. [The FG syndrome (McK 30545). Description of 2 cases with subaortic stenosis].
    Russo A; Lanna P; Perna GP; Salvatori MP; Villella A; Fanelli R
    G Ital Cardiol; 1985 Mar; 15(3):349-53. PubMed ID: 4040487
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Cayler's cardio-facial syndrome. Apropos of 19 cases].
    Perrin P; Worms AM; Marçon F; Perrin C; Pernot C
    Arch Fr Pediatr; 1989 Apr; 46(4):257-61. PubMed ID: 2665683
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries.
    Balci S; Haytoğlu T; Ozer S
    Turk J Pediatr; 1998; 40(3):461-6. PubMed ID: 9763914
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Craniosynostosis and kidney malformation in a case of Hennekam syndrome.
    Cormier-Daire V; Lyonnet S; Lehnert A; Martin D; Salomon R; Patey N; Broyer M; Ricour C; Munnich A
    Am J Med Genet; 1995 May; 57(1):66-8. PubMed ID: 7645602
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome?
    Wilkie AO; Taylor D; Scambler PJ; Baraitser M
    Clin Dysmorphol; 1993 Apr; 2(2):114-9. PubMed ID: 8281271
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal growth retardation, microcephaly, and eye coloboma in infant with multiple congenital anomalies: further delineation of presumed new dysmorphic syndrome.
    Cuturilo G; Jovanovic I; Vukomanovic G; Djukic M; Stefanovic I; Atanskovic-Markovic M
    Birth Defects Res A Clin Mol Teratol; 2008 Mar; 82(3):166-8. PubMed ID: 18232021
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML; Pai GS; Wilkes B; Lebel RR
    Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Distichiasis-lymphedema. A hereditary syndrome of multiple congenital defects.
    Robinow M; Johnson GF; Verhagen AD
    Am J Dis Child; 1970 Apr; 119(4):343-7. PubMed ID: 5434594
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.