BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 2840828)

  • 1. Expanding the spectrum of the Perlman syndrome.
    Greenberg F; Copeland K; Gresik MV
    Am J Med Genet; 1988 Apr; 29(4):773-6. PubMed ID: 2840828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Perlman familial nephroblastomatosis syndrome.
    Greenberg F; Stein F; Gresik MV; Finegold MJ; Carpenter RJ; Riccardi VM; Beaudet AL
    Am J Med Genet; 1986 May; 24(1):101-10. PubMed ID: 3010722
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Perlman syndrome: four additional cases and review.
    Henneveld HT; van Lingen RA; Hamel BC; Stolte-Dijkstra I; van Essen AJ
    Am J Med Genet; 1999 Oct; 86(5):439-46. PubMed ID: 10508986
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare clinical entity Perlman syndrome: is cholestasis a new finding?
    Demirel G; Oguz SS; Celik IH; Uras N; Erdeve O; Dilmen U
    Congenit Anom (Kyoto); 2011 Mar; 51(1):43-5. PubMed ID: 20726997
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Perlman syndrome: report of a case with additional radiographic findings.
    Herman TE; McAlister WH
    Pediatr Radiol; 1995 Nov; 25 Suppl 1():S70-2. PubMed ID: 8577560
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diaphragmatic hernia in the Coffin-Siris syndrome.
    Delvaux V; Moerman P; Fryns JP
    Genet Couns; 1998; 9(1):45-50. PubMed ID: 9555587
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical-genealogic analysis of diaphragmatic hernias].
    Il'ina EG
    Genetika; 1992 Jul; 28(7):165-71. PubMed ID: 1427052
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perlman syndrome: report, prenatal findings and review.
    Alessandri JL; Cuillier F; Ramful D; Ernould S; Robin S; de Napoli-Cocci S; Rivière JP; Rossignol S
    Am J Med Genet A; 2008 Oct; 146A(19):2532-7. PubMed ID: 18780370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An infant with diaphragmatic hernia, anophthalmia and cardiac defect: evaluation by magnetic resonance imaging autopsy.
    Ceylaner S; Gozer HE; Ceylaner G; Ertas IE; Kizilates SU; Edguer T
    Genet Couns; 2006; 17(2):231-6. PubMed ID: 16970042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. "C" trigonocephaly syndrome with diaphragmnatic hernia.
    Addor MC; Stefanutti D; Farron F; Meinecke P; Lacombe D; Sarlangue J; Prescia G; Schorderet DF
    Genet Couns; 1995; 6(2):113-20. PubMed ID: 7546453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies.
    Neri G; Martini-Neri ME; Katz BE; Opitz JM
    Am J Med Genet; 1984 Sep; 19(1):195-207. PubMed ID: 6093533
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fryns syndrome in children with congenital diaphragmatic hernia.
    Neville HL; Jaksic T; Wilson JM; Lally PA; Hardin WD; Hirschl RB; Langham MR; Lally KP;
    J Pediatr Surg; 2002 Dec; 37(12):1685-7. PubMed ID: 12483630
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fryns syndrome: a lethal mesoectodermal birth defect with variable expression in a pair of monozygotic twins.
    Pratap A; Agrawal A; Raja S; Khaniya S; Tiwari A; Kumar A
    Singapore Med J; 2007 Apr; 48(4):e106-8. PubMed ID: 17384863
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bilateral congenital diaphragmatic hernia.
    Neville HL; Jaksic T; Wilson JM; Lally PA; Hardin WD; Hirschl RB; Lally KP;
    J Pediatr Surg; 2003 Mar; 38(3):522-4. PubMed ID: 12632380
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Associated malformations in cases with congenital diaphragmatic hernia.
    Stoll C; Alembik Y; Dott B; Roth MP
    Genet Couns; 2008; 19(3):331-9. PubMed ID: 18990989
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia.
    Vasudevan PC; Twigg SR; Mulliken JB; Cook JA; Quarrell OW; Wilkie AO
    Eur J Hum Genet; 2006 Jul; 14(7):884-7. PubMed ID: 16639408
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL; Bixler D; Girod D
    Am J Med Genet; 1983 Sep; 16(1):35-42. PubMed ID: 6638068
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.
    Moerman P; Fryns JP; Vandenberghe K; Devlieger H; Lauweryns JM
    Am J Med Genet; 1988 Dec; 31(4):805-14. PubMed ID: 3239572
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of Perlman syndrome presenting with hemorrhagic hemangioma.
    Pirgon O; Atabek ME; Akin F; Sert A
    J Pediatr Hematol Oncol; 2006 Aug; 28(8):531-3. PubMed ID: 16912594
    [TBL] [Abstract][Full Text] [Related]  

  • 20. McKusick-Kaufman syndrome: report of an instructive family.
    Vince JD; Martin NJ
    Am J Med Genet; 1989 Feb; 32(2):174-7. PubMed ID: 2564737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.