BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 2333881)

  • 1. Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?
    Farag TI; Teebi AS
    Am J Med Genet; 1990 Apr; 35(4):516-8. PubMed ID: 2333881
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive Robinow syndrome.
    Teebi AS
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of Opitz (BBB) syndrome in the second trimester by ultrasound detection of hypospadias and hypertelorism.
    Hogdall C; Siegel-Bartelt J; Toi A; Ritchie S
    Prenat Diagn; 1989 Nov; 9(11):783-93. PubMed ID: 2694153
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Variable expression of an autosomal dominant syndrome: (BBB syndrome or G syndrome)].
    Le Merrer M; Verloes A; Narcy P; Briard ML
    J Genet Hum; 1988 Jun; 36(3):257-64. PubMed ID: 3411306
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Severe hypertelorism, midface prominence, prominent/simple ears, severe myopia, borderline intelligence, and bone fragility in two brothers: new syndrome?
    Hamamy HA; Teebi AS; Oudjhane K; Shegem NN; Ajlouni KM
    Am J Med Genet A; 2007 Feb; 143A(3):229-34. PubMed ID: 17230486
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Uncomplicated familial hypospadias: evidence for autosomal recessive inheritance.
    Frydman M; Greiber C; Cohen HA
    Am J Med Genet; 1985 May; 21(1):51-60. PubMed ID: 4003448
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome.
    Stoll C; Geraudel A; Berland H; Roth MP; Dott B
    Am J Med Genet; 1985 Feb; 20(2):221-5. PubMed ID: 4038851
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?
    Lammer EJ; Scholes T; Abrams L
    Clin Dysmorphol; 2001 Jan; 10(1):9-13. PubMed ID: 11152158
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Opitz hypertelorism-hypospadias syndrome. Further delineation of the spectrum of clinical findings.
    Dereymaeker AM; Fryns JP; Hoefnagels M; Heremans G; Marien J; Van den Berghe H
    J Genet Hum; 1987 Aug; 35(4):259-65. PubMed ID: 3655750
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The G and BBB syndromes: case presentations, genetics, and nosology.
    Funderburk SJ; Stewart R
    Am J Med Genet; 1978; 2(2):131-44. PubMed ID: 263433
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Tetralogy of Fallot with pulmonary atresia in siblings.
    Der Kaloustian VM; Ratl H; Malouf J; Hatem J; Slim M; Tomeh A; Khouri J; Kutayli F
    Am J Med Genet; 1985 May; 21(1):119-22. PubMed ID: 4003436
    [TBL] [Abstract][Full Text] [Related]  

  • 13. G syndrome: an unusual family.
    Allanson JE
    Am J Med Genet; 1988 Nov; 31(3):637-42. PubMed ID: 3228142
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hypertelorism-hypospadias (BBB) syndrome. 2 additional family studies].
    Krause M; Meinecke P; Krins M; Grote W
    Monatsschr Kinderheilkd; 1990 Jan; 138(1):31-3. PubMed ID: 2314402
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A familial disorder with duodenal atresia and tetralogy of Fallot.
    Lemire EG; Evans JA; Giddins NG; Harman CR; Wiseman NE; Chudley AE
    Am J Med Genet; 1996 Dec; 66(1):39-44. PubMed ID: 8957509
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new hypospadias-mental retardation syndrome in three brothers.
    Goldblatt J; Wallis C; Viljoen D
    Am J Dis Child; 1987 Nov; 141(11):1168-9. PubMed ID: 3673966
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypertelorism, proptosis, ptosis, polysyndactyly, hypospadias and normal height in 3 sibs: a new syndrome?
    Naguib KK
    Am J Med Genet; 1988 Jan; 29(1):35-41. PubMed ID: 2830788
    [No Abstract]   [Full Text] [Related]  

  • 18. Hypertelorism-microtia-clefting (HMC) syndrome.
    Verloes A
    Genet Couns; 1994; 5(3):283-7. PubMed ID: 7811429
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frontonasal dysplasia associated with tetralogy of Fallot.
    De Moor MM; Baruch R; Human DG
    J Med Genet; 1987 Feb; 24(2):107-9. PubMed ID: 3560167
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
    Donnai D; Barrow M
    Am J Med Genet; 1993 Oct; 47(5):679-82. PubMed ID: 8266995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.