BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 6335367)

  • 1. [Association of VACTERL and hydrocephalus: a new familial entity].
    Briard ML; le Merrer M; Plauchu H; Dodinval P; Lambotte C; Moraine C; Serville F
    Ann Genet; 1984; 27(4):220-3. PubMed ID: 6335367
    [TBL] [Abstract][Full Text] [Related]  

  • 2. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.
    Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D
    Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X-linked VACTERL with hydrocephalus: the VACTERL-H syndrome.
    Genuardi M; Chiurazzi P; Capelli A; Neri G
    Birth Defects Orig Artic Ser; 1993; 29(1):235-41. PubMed ID: 8280876
    [No Abstract]   [Full Text] [Related]  

  • 4. [Association of hereditary hydrocephalus and holoprosencephaly].
    Lambert JC; Ferrari M; Donzeau M; Hericort P; Boutte P; Walbaum R; Ayraud N
    Arch Fr Pediatr; 1983 May; 40(5):397-9. PubMed ID: 6882130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaicism?
    Orstavik KH; Steen-Johnsen J; Foerster A; Fjeld T; Skullerud K; Lie SO
    Am J Med Genet; 1992 Aug; 43(6):1035-8. PubMed ID: 1415331
    [TBL] [Abstract][Full Text] [Related]  

  • 6. VACTERL with hydrocephalus: further delineation of the syndrome(s).
    Evans JA; Stranc LC; Kaplan P; Hunter AG
    Am J Med Genet; 1989 Oct; 34(2):177-82. PubMed ID: 2816994
    [TBL] [Abstract][Full Text] [Related]  

  • 7. VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
    Porteous ME; Cross I; Burn J
    Am J Med Genet; 1992 Aug; 43(6):1032-4. PubMed ID: 1415330
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance.
    Aymé S; Mattei JF
    Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616
    [TBL] [Abstract][Full Text] [Related]  

  • 9. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.
    Corsello G; Giuffrè L
    Am J Med Genet; 1994 Jan; 49(1):137-8. PubMed ID: 8172244
    [No Abstract]   [Full Text] [Related]  

  • 10. Absence of excess chromosome breakage in a patient with VACTERL-hydrocephalus.
    Evans JA; Chodirker BN
    Am J Med Genet; 1993 Aug; 47(1):112-3. PubMed ID: 8240537
    [No Abstract]   [Full Text] [Related]  

  • 11. VACTERL with hydrocephalus and branchial arch defects: prenatal, clinical, and autopsy findings in two brothers.
    Froster UG; Wallner SJ; Reusche E; Schwinger E; Rehder H
    Am J Med Genet; 1996 Mar; 62(2):169-72. PubMed ID: 8882398
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.
    Rossbach HC; Sutcliffe MJ; Haag MM; Grana NH; Rossi AR; Barbosa JL
    Am J Med Genet; 1996 Jan; 61(1):65-7. PubMed ID: 8741921
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial hydrocephalus, recessive hereditary gonosomic disease (Bickers and Adams syndrome)].
    Martin C; Got M; Babin JP; Cazauran JM
    Arch Fr Pediatr; 1971 Nov; 28(9):971-4. PubMed ID: 5144696
    [No Abstract]   [Full Text] [Related]  

  • 14. VACTERL with hydrocephalus and isolated tracheo-oesophageal fistula in a first cousin.
    Grech V; Fearne C; Parascandalo R; Soler P
    Clin Dysmorphol; 2000 Apr; 9(2):145-6. PubMed ID: 10826631
    [TBL] [Abstract][Full Text] [Related]  

  • 15. VACTERL with hydrocephalus. A distinct entity with a variable spectrum of multiple congenital anomalies.
    Vandenborre K; Beemer F; Fryns JP; Vandenborne K [corrected to Vandenborre K]
    Genet Couns; 1993; 4(3):199-201. PubMed ID: 8267927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial hydrocephalus of prenatal onset.
    Zlotogora J; Sagi M; Cohen T
    Am J Med Genet; 1994 Jan; 49(2):202-4. PubMed ID: 8116668
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome.
    Holden ST; Cox JJ; Kesterton I; Thomas NS; Carr C; Woods CG
    J Med Genet; 2006 Sep; 43(9):750-4. PubMed ID: 16679491
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The hydrolethalus syndrome--a new hereditary malformation syndrome in Finland].
    Salonen R; Herva R; Norio R
    Duodecim; 1981; 97(16):1312-9. PubMed ID: 7327122
    [No Abstract]   [Full Text] [Related]  

  • 19. [Autosomal recessive inheritance of hydrocephalus with stenosis of the duct of Sylvius].
    Petrus M; Dutau G; Rochiccioli P
    J Genet Hum; 1981 Jun; 29(2):155-60. PubMed ID: 7328410
    [No Abstract]   [Full Text] [Related]  

  • 20. VACTERL with the mitochondrial np 3243 point mutation.
    Damian MS; Seibel P; Schachenmayr W; Reichmann H; Dorndorf W
    Am J Med Genet; 1996 Apr; 62(4):398-403. PubMed ID: 8723071
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.