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3. The Meckel syndrome: clinicopathological findings in 67 patients. Salonen R Am J Med Genet; 1984 Aug; 18(4):671-89. PubMed ID: 6486167 [TBL] [Abstract][Full Text] [Related]
4. Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome. Mecke S; Passarge E Ann Genet; 1971 Jun; 14(2):97-103. PubMed ID: 4997715 [No Abstract] [Full Text] [Related]
5. Cystic kidney dysplasia and polydactyly in 3 sibs with Bardet-Biedl syndrome. Gershoni-Baruch R; Nachlieli T; Leibo R; Degani S; Weissman I Am J Med Genet; 1992 Oct; 44(3):269-73. PubMed ID: 1488972 [TBL] [Abstract][Full Text] [Related]
6. Cerebro-reno-digital syndrome in two sibs. Piantanida M; Tiberti A; Plebani A; Martelli P; Danesino C Am J Med Genet; 1993 Sep; 47(3):420-2. PubMed ID: 8135292 [TBL] [Abstract][Full Text] [Related]
7. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs. Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046 [TBL] [Abstract][Full Text] [Related]
8. Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Hsia YE; Bratu M; Herbordt A Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860 [No Abstract] [Full Text] [Related]
9. The neurofaciodigitorenal (NFDR) syndrome. Freire-Maia N; Pinheiro M; Opitz JM Am J Med Genet; 1982 Mar; 11(3):329-36. PubMed ID: 7081297 [TBL] [Abstract][Full Text] [Related]
10. Meckel syndrome with Caroli disease and choledochal cysts. Venkatachala S; Sivaraman A Fetal Pediatr Pathol; 2011; 30(5):350-4. PubMed ID: 21843058 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. New autosomal-recessive syndrome of Leber congenital amaurosis, short stature, growth hormone insufficiency, mental retardation, hepatic dysfunction, and metabolic acidosis. Ehara H; Nakano C; Ohno K; Goto YI; Takeshita K Am J Med Genet; 1997 Aug; 71(3):258-66. PubMed ID: 9268092 [TBL] [Abstract][Full Text] [Related]
14. The Meckel syndrome in Finland: epidemiologic and genetic aspects. Salonen R; Norio R Am J Med Genet; 1984 Aug; 18(4):691-8. PubMed ID: 6486168 [TBL] [Abstract][Full Text] [Related]
15. Dandy-Walker malformation in the Meckel syndrome. Herriot R; Hallam LA; Gray ES Am J Med Genet; 1991 May; 39(2):207-10. PubMed ID: 2063927 [TBL] [Abstract][Full Text] [Related]
16. [Prenatal diagnosis of Meckel's syndrome in a family]. Degenhardt F; Mühlhaus K Ultraschall Med; 1985 Aug; 6(4):226-8. PubMed ID: 3903995 [TBL] [Abstract][Full Text] [Related]
17. Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome? Pitt DB; Rogers JG; Danks DM Am J Med Genet; 1984 Oct; 19(2):307-13. PubMed ID: 6542309 [TBL] [Abstract][Full Text] [Related]
18. Syndrome of mental retardation and distal arthrogryposis in sibs. Chitayat D; Hodgkinson KA; Blaichman S; Chen ME; Watters GV; Khalife S; Hall JG Am J Med Genet; 1991 Oct; 41(1):49-51. PubMed ID: 1951463 [TBL] [Abstract][Full Text] [Related]