BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 9450888)

  • 1. Karsch-Neugebauer syndrome in two sibs with unaffected parents.
    Wong SC; Cobben JM; Hiemstra S; Robinson PH; Heeg M
    Am J Med Genet; 1998 Jan; 75(2):207-10. PubMed ID: 9450888
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Karsch-Neugebauer syndrome: split foot/split hand and congenital nystagmus.
    Pilarski RT; Pauli RM; Bresnick GH; Lebovitz RM
    Clin Genet; 1985 Jan; 27(1):97-101. PubMed ID: 3978843
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father.
    De Smet L; Devriendt K; Fryns JP
    Genet Couns; 2001; 12(3):251-4. PubMed ID: 11693788
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital heart defects, hamartomas of the tongue and polysyndactyly in a sister and brother.
    Orstavik KH; Lindemann R; Solberg LA; Foerster A; Sørland SJ
    Clin Genet; 1992 Jul; 42(1):19-21. PubMed ID: 1516223
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dilemmas in counselling: the EEC syndrome.
    Tse K; Temple IK; Baraitser M
    J Med Genet; 1990 Dec; 27(12):752-5. PubMed ID: 2074560
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Acro-cardio-facial syndrome: a microdeletion syndrome?
    Toschi B; Valetto A; Bertini V; Congregati C; Cantinotti M; Assanta N; Simi P
    Am J Med Genet A; 2012 Aug; 158A(8):1994-9. PubMed ID: 22740423
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A; Ferrareto I; Masiero D; da Silva CR
    Am J Med Genet; 1987 Aug; 27(4):867-84. PubMed ID: 3425598
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A; Donnai D
    Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family.
    Richieri-Costa A; de Miranda E; Kamiya TY; Freire-Maia DV
    Am J Med Genet; 1990 May; 36(1):1-6. PubMed ID: 2333896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1.
    Marinoni JC; Boyd E; Sherman S; Schwartz C
    Hum Mol Genet; 1994 Aug; 3(8):1355-7. PubMed ID: 7987314
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Anomalous inheritance in a kindred with split hand, split foot malformation.
    Spranger M; Schapera J
    Eur J Pediatr; 1988 Feb; 147(2):202-5. PubMed ID: 3366140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES; Richieri-Costa A
    Am J Med Genet; 1990 Sep; 37(1):42-53. PubMed ID: 2240042
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A split hand-split foot (SHFM3) gene is located at 10q24-->25.
    Gurrieri F; Prinos P; Tackels D; Kilpatrick MW; Allanson J; Genuardi M; Vuckov A; Nanni L; Sangiorgi E; Garofalo G; Nunes ME; Neri G; Schwartz C; Tsipouras P
    Am J Med Genet; 1996 Apr; 62(4):427-36. PubMed ID: 8723077
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term follow-up of two sibs with Larsen syndrome possibly due to parental germ-line mosaicism.
    Petrella R; Rabinowitz JG; Steinmann B; Hirschhorn K
    Am J Med Genet; 1993 Aug; 47(2):187-97. PubMed ID: 8213905
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Counseling dilemmas in EEC syndrome.
    Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J
    Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA; D'Agostino S; Costa L; Musi L; Cappellari F
    Pediatr Med Chir; 1997; 19(2):121-4. PubMed ID: 9312747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes.
    Lacombe D; Serville F; Marchand D; Battin J
    J Med Genet; 1993 Aug; 30(8):700-3. PubMed ID: 8411061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.
    Tackels-Horne D; Toburen A; Sangiorgi E; Gurrieri F; de Mollerat X; Fischetto R; Causio F; Clarkson K; Stevenson RE; Schwartz CE
    Clin Genet; 2001 Jan; 59(1):28-36. PubMed ID: 11168022
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Acheiropody. A report of two cases.
    Kruger LM; Kumar A
    J Bone Joint Surg Am; 1994 Oct; 76(10):1557-60. PubMed ID: 7929505
    [No Abstract]   [Full Text] [Related]  

  • 20. Hand-foot-genital syndrome: the importance of hallux varus.
    Cleveland RH; Holmes LB
    Pediatr Radiol; 1990; 20(5):339-43. PubMed ID: 2349017
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.