BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 1785638)

  • 1. Weaver syndrome in two Japanese children.
    Kondo I; Mori Y; Kuwajima K
    Am J Med Genet; 1991 Nov; 41(2):221-4. PubMed ID: 1785638
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
    Weidle B; Orstavik KH
    Tidsskr Nor Laegeforen; 1998 Apr; 118(10):1556-8. PubMed ID: 9615582
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.
    Garganta CL; Bodurtha JN
    Am J Med Genet; 1992 Sep; 44(2):129-35. PubMed ID: 1456279
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
    Terespolsky D; Farrell SA; Siegel-Bartelt J; Weksberg R
    Am J Med Genet; 1995 Nov; 59(3):329-33. PubMed ID: 8599356
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ
    Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiple odontogenic keratocysts in mental retardation-overgrowth (Simpson-Golabi-Behmel) syndrome.
    Krimmel M; Reinert S
    Br J Oral Maxillofac Surg; 2000 Jun; 38(3):221-3. PubMed ID: 10864729
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutchinick syndrome in a Japanese girl.
    Tonoki H; Hattori T; Kamoshida H; Ohta Y; Niikawa N
    Am J Med Genet; 1999 Mar; 83(2):96-9. PubMed ID: 10190479
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B; Ulmer H; Müller U
    Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Report on two patients with Costello syndrome and sialuria.
    Di Rocco M; Gatti R; Gandullia P; Barabino A; Picco P; Borrone C
    Am J Med Genet; 1993 Nov; 47(7):1135-40. PubMed ID: 8291534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Natural history of mosaic trisomy 14 syndrome.
    Fujimoto A; Allanson J; Crowe CA; Lipson MH; Johnson VP
    Am J Med Genet; 1992 Sep; 44(2):189-96. PubMed ID: 1456290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The Simpson-Golabi-Behmel syndrome. The stages of a diagnostic procedure].
    Di Rocco M; Lignana E; Faraci M; Leveratto L; Borrone C
    Minerva Pediatr; 1993 Apr; 45(4):163-7. PubMed ID: 8355647
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC; Geerdink RA; Hamel BC; Hennekam FA; Kraus P; Rammeloo JA; Tillemans AA
    Am J Med Genet; 1989 Dec; 34(4):593-600. PubMed ID: 2624276
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Floating Harbor syndrome. Case report and further syndrome delineation.
    Midro AT; Olchowik B; Rogowska M; Hubert E; Hassman-Poznańska E; Papasz A; Szulc S; Wiśniewski A
    Ann Genet; 1997; 40(3):133-8. PubMed ID: 9401100
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel findings in a patient with Weaver or a Weaver-like syndrome.
    Scarano G; Della Monica M; Lonardo F; Neri G
    Am J Med Genet; 1996 May; 63(2):378-81. PubMed ID: 8725789
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Weaver syndrome. 1st case reported in Venezuela].
    Sánchez O; Boufajreldin S; Oranges C; Orta C; Guerra D
    Invest Clin; 1997 Mar; 38(1):9-24. PubMed ID: 9235073
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA; García-Cruz D; García-Cruz O; Sánchez-Corona J
    Am J Med Genet; 1995 Feb; 55(4):420-2. PubMed ID: 7762580
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation.
    Morillo-Cucci G; Passarge E; Simpson JL; Chaganti RS; German J
    Birth Defects Orig Artic Ser; 1975; 11(2):380-3. PubMed ID: 1227554
    [No Abstract]   [Full Text] [Related]  

  • 19. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS; Wisniewski K; Brown WT
    Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
    Gurrieri F; Cappa M; Neri G
    Am J Med Genet; 1992 Sep; 44(2):136-7. PubMed ID: 1456280
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.