602 related articles for article (PubMed ID: 4997860)
1. 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]
2. The Roberts syndrome.
Freeman MV; Williams DW; Schimke RN; Temtamy SA; Vachier E; German J
Birth Defects Orig Artic Ser; 1974; 10(5):87-95. PubMed ID: 4220010
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Meckel-Gruber syndrome.
Ramachandran U; Malla T; Joshi KS
Kathmandu Univ Med J (KUMJ); 2006; 4(3):334-6. PubMed ID: 18603929
[TBL] [Abstract][Full Text] [Related]
5. [2 new cases of Meckel-Gruber syndrome in the same family].
Franzoni R; Scalercio A
Minerva Pediatr; 1986 Sep; 38(17-18):783-9. PubMed ID: 3796537
[No Abstract] [Full Text] [Related]
6. Familial holoprosencephaly.
Dallaire L; Fraser FC; Wiglesworth FW
Birth Defects Orig Artic Ser; 1971 Jun; 7(7):136-42. PubMed ID: 5173201
[TBL] [Abstract][Full Text] [Related]
7. Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.
Fried K; Liban E; Lurie M; Friedman S; Reisner SH
J Med Genet; 1971 Sep; 8(3):285-90. PubMed ID: 4999589
[No Abstract] [Full Text] [Related]
8. Walker-Warburg syndrome with cleft lip and cleft palate in two sibs.
Burton BK; Dillard RG; Weaver RG
Am J Med Genet; 1987 Jul; 27(3):537-41. PubMed ID: 3631127
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defects.
Gillessen-Kaesbach G; Meinecke P; Garrett C; Padberg BC; Rehder H; Passarge E
Am J Med Genet; 1993 Feb; 45(4):511-8. PubMed ID: 8465860
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
McPherson E; Clemens M
Am J Med Genet; 1996 Mar; 62(1):58-60. PubMed ID: 8779326
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. [Tetrasomy 9p].
Foerster W; Koch M; Hansen S
Monatsschr Kinderheilkd; 1985 Sep; 133(9):694-7. PubMed ID: 2865673
[TBL] [Abstract][Full Text] [Related]
17. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings.
Neu RL; Kajii T; Gardner LI; Nagyfy SF
Pediatrics; 1971 Mar; 47(3):610-2. PubMed ID: 5547878
[No Abstract] [Full Text] [Related]
18. New manifestations in an infant with Neu Laxova syndrome.
Rouzbahani L
Am J Med Genet; 1995 Mar; 56(2):239-40. PubMed ID: 7625453
[No Abstract] [Full Text] [Related]
19. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
Bartsocas CS; Papas CV
J Med Genet; 1972 Jun; 9(2):222-6. PubMed ID: 4339984
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
