BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 7246621)

  • 21. [The Meckel syndrome (author's transl)].
    Leucht W; Heyes H; Müller E; Schmidt W
    Geburtshilfe Frauenheilkd; 1981 Nov; 41(11):765-8. PubMed ID: 6172316
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Phenotypic variation in Meckel syndrome.
    Seller MJ
    Clin Genet; 1981 Jul; 20(1):74-7. PubMed ID: 7296953
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cerebral malformation, seizures, hypertrichosis, distinct face, claw hands, and overlapping fingers in sibs of both sexes.
    Müller FM; Barth GM; Menger H; Spranger J
    Am J Med Genet; 1993 Oct; 47(5):698-701. PubMed ID: 8266998
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Polydactyly in a carrier of the gene for the Meckel syndrome.
    Nelson J; Nevin NC; Hanna EJ
    Am J Med Genet; 1994 Nov; 53(3):207-9. PubMed ID: 7856653
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Phenotypic variability in Meckel-Gruber syndrome.
    Farag TI; Usha R; Uma R; Mady SA; al-Nagdy K; el-Badramany MH
    Clin Genet; 1990 Sep; 38(3):176-9. PubMed ID: 2225527
    [TBL] [Abstract][Full Text] [Related]  

  • 28. von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.
    Lubinsky MS; Kahler SG; Speer IE; Hoyme HE; Kirillova IA; Lurie IW
    Am J Med Genet; 1994 Sep; 52(3):272-8. PubMed ID: 7810558
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Meckel syndrome in 2 brothers. Clinical, anatomopathologic and genetic aspects].
    Restrepo CM; García-Cruz D; Sánchez G; Cantú JM
    Bol Med Hosp Infant Mex; 1988 Sep; 45(9):600-4. PubMed ID: 3190852
    [No Abstract]   [Full Text] [Related]  

  • 30. Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gestation.
    Balci S; Tekşen F; Dökmeci F; Cengiz B; Cömert RB; Can B; Ozdamar S
    Turk J Pediatr; 2004; 46(3):283-8. PubMed ID: 15503488
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The Meckel syndrome: report of two Japanese sibs and a review of literature.
    Sugiura Y; Suzuki Y; Kobayashi M
    Am J Med Genet; 1996 May; 67(3):312-4. PubMed ID: 8725749
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Study of the malformation of ductal plate of the liver in Meckel syndrome and review of other syndromes presenting with this anomaly.
    Sergi C; Adam S; Kahl P; Otto HF
    Pediatr Dev Pathol; 2000; 3(6):568-83. PubMed ID: 11000335
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Brain pathology in the Meckel syndrome: a study of 59 cases.
    Paetau A; Salonen R; Haltia M
    Clin Neuropathol; 1985; 4(2):56-62. PubMed ID: 3995807
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Combination of cor triatriatum sinistrum and hypoplastic left heart syndrome in Meckel-Gruber syndrome: a case report.
    Taweevisit M; Treetipsatit J; Tantbirojn P; Thorner PS
    Pediatr Dev Pathol; 2009; 12(5):404-9. PubMed ID: 19358626
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis of Meckel syndrome.
    Fryns JP; Vandenberghe K; Van Assche FA; Cassiman JJ; van den Berghe H
    J Genet Hum; 1980 Dec; 28(4):89-94. PubMed ID: 7205201
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cerebro-reno-digital (Meckel-like) syndrome with Dandy-Walker malformation, cystic kidneys, hepatic fibrosis, and polydactyly.
    Genuardi M; Dionisi-Vici C; Sabetta G; Mignozzi M; Rizzoni G; Cotugno G; Martini Neri ME
    Am J Med Genet; 1993 Aug; 47(1):50-3. PubMed ID: 8368252
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Etiologic heterogeneity of neural-tube defects.
    Holmes LB; Driscoll SG; Atkins L
    N Engl J Med; 1976 Feb; 294(7):365-9. PubMed ID: 1107843
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Skeletal abnormalities in Meckel syndrome.
    Shanks J; Kerr B; Russell SA; Kingston H; Moore L
    Pediatr Pathol Lab Med; 1997; 17(4):625-30. PubMed ID: 9211556
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome.
    Frank V; den Hollander AI; Brüchle NO; Zonneveld MN; Nürnberg G; Becker C; Du Bois G; Kendziorra H; Roosing S; Senderek J; Nürnberg P; Cremers FP; Zerres K; Bergmann C
    Hum Mutat; 2008 Jan; 29(1):45-52. PubMed ID: 17705300
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Meckel syndrome. Difficulties in prenatal diagnosis caused by variability of expression (observations on two families)].
    Plauchu H; Kemlin I; Bouvier R; Robert JM
    J Genet Hum; 1981 Dec; 29(4):431-40. PubMed ID: 7328417
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.