BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 1749628)

  • 21. The McKusick-Kaufman syndrome: recessively inherited vaginal atresia, hydrometrocolpos, uterovaginal duplications, anorectal anomalies, postaxial polydactyly, and congenital heart disease.
    Robinow M; Shaw A
    J Pediatr; 1979 May; 94(5):776-8. PubMed ID: 448491
    [No Abstract]   [Full Text] [Related]  

  • 22. [McKusick-Kaufman syndrome as a cause of acute abdomen in the neonatal period].
    Franke B; Missbach D; Römer KH
    Zentralbl Chir; 1988; 113(4):254-8. PubMed ID: 3364056
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The McKusick-Kaufman hydrometrocolpos-polydactyly syndrome--a case report.
    Hsu YR; Chuang JH; Huang CB; Changchien CC
    Changgeng Yi Xue Za Zhi; 1994 Jun; 17(2):173-7. PubMed ID: 8069743
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial holoprosencephaly, heart defects, and polydactyly.
    Hennekam RC; van Noort G; de la Fuente AA
    Am J Med Genet; 1991 Nov; 41(2):258-62. PubMed ID: 1785646
    [TBL] [Abstract][Full Text] [Related]  

  • 25. McKusick-Kaufman syndrome: the diagnostic challenge of abdominal distension in the neonatal period.
    Schaap C; de Die-Smulders CE; Kuijten RH; Fryns JP
    Eur J Pediatr; 1992 Aug; 151(8):583-5. PubMed ID: 1505577
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
    Santos H; Cordeiro I; Medeira A; Mendonça E; Antunes NL; Rosa FC
    Genet Couns; 1994; 5(2):187-9. PubMed ID: 7917131
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Case report of Laurence-Moon-Bardet-Biedl syndrome].
    Osusky R; Alsaadi AH; Farpour H
    Klin Monbl Augenheilkd; 1991 May; 198(5):445-6. PubMed ID: 1886381
    [TBL] [Abstract][Full Text] [Related]  

  • 28. McKusick-Kaufman syndrome associated with esophageal atresia and distal tracheoesophageal fistula: a case report and review of the literature.
    Pul N; Pul M; Gedik Y
    Am J Med Genet; 1994 Feb; 49(3):341-3. PubMed ID: 8209897
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly".
    Fraser FC; Lytwyn A
    Am J Med Genet; 1981; 9(1):67-73. PubMed ID: 7246621
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphy.
    Stoll C; Finck S; Janser B; Printz M; Lutz P
    Genet Couns; 1992; 3(1):41-7. PubMed ID: 1590980
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hydrometrocolpos, postaxial polydactyly, congenital heart disease, and anomalies of the gastrointestinal and genitourinary tracts: a rare autosomal recessive syndrome.
    Goecke T; Dopfer R; Huenges R; Conzelmann W; Feller A; Majewski F
    Eur J Pediatr; 1981 Jul; 136(3):297-305. PubMed ID: 7262101
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M
    Genet Couns; 1994; 5(4):345-55. PubMed ID: 7888136
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Fountain syndrome: further delineation of the clinical syndrome and follow-up data.
    Van Buggenhout GJ; Van Ravenswaaij-Arts CM; Renier WO; Van de Wiel MP; Trommelen JC; Pijkels E; Hamel BC; Fryns JP
    Genet Couns; 1996; 7(3):177-86. PubMed ID: 8897038
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
    Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Complex cyanotic heart defect in a newborn infant with cat eye syndrome].
    Paul T; Reimer A; Wilken M; Miller K; Kallfelz HC
    Monatsschr Kinderheilkd; 1991 Apr; 139(4):228-30. PubMed ID: 2072964
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
    [No Abstract]   [Full Text] [Related]  

  • 37. [A fatal autosomal recessive syndrome with multiple congenital contractures].
    Herva R; Leisti J; Kirkinen P; Seppänen U; Martikainen J
    Duodecim; 1985; 101(8):756-62. PubMed ID: 4039655
    [No Abstract]   [Full Text] [Related]  

  • 38. Antley-Bixler syndrome: case report and review of the literature.
    Poddevin F; Delobel B; Courreges P; Bayart M
    Genet Couns; 1995; 6(3):241-6. PubMed ID: 8588853
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Unusual presentation of McKusick-Kaufman syndrome in a female Bedouin Arab baby.
    Kawar B; Sakran W; Chervinsky L; Siplovich L
    Eur J Pediatr Surg; 2005 Dec; 15(6):446-8. PubMed ID: 16418967
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pallister-Hall syndrome and McKusick-Kaufmann syndrome: one entity?
    Unsinn KM; Neu N; Krejci A; Posch A; Menardi G; Gassner I
    J Med Genet; 1995 Feb; 32(2):125-8. PubMed ID: 7760322
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.