112 related articles for article (PubMed ID: 8471221)
1. Macrocephaly and mental retardation. The unique association with short stature, spastic paraplegia and CNS malformations.
Volcke P; Soekarman D; Vandenbussche P; Haegeman J; Smeets E; Thiry P; Fryns JP
Genet Couns; 1993; 4(1):47-50. PubMed ID: 8471221
[TBL] [Abstract][Full Text] [Related]
2. Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy.
Di Rocco M; Leveratto L; Cama A; Bado M; Tortori Donati P; Andreussi L; Borrone C
Genet Couns; 1993; 4(4):295-8. PubMed ID: 8110418
[TBL] [Abstract][Full Text] [Related]
3. Distinct familial syndrome of severe to profound mental retardation, spastic paraplegia with contrasting axial hypotonia, short stature and distinct craniofacial appearance with nasal hypoplasia.
Fryns JP; Devriendt K; Detroch C; Decock P
Genet Couns; 1998; 9(1):51-4. PubMed ID: 9555588
[No Abstract] [Full Text] [Related]
4. An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation.
Buttiens M; Fryns JP; van den Berghe H
Clin Genet; 1989 Dec; 36(6):451-55. PubMed ID: 2591071
[TBL] [Abstract][Full Text] [Related]
5. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
Ritscher D; Schinzel A; Boltshauser E; Briner J; Arbenz U; Sigg P
Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
[TBL] [Abstract][Full Text] [Related]
6. Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.
Fryns JP; Vogels A; Haegeman J; Eggermont E; van den Berghe H
Genet Couns; 1994; 5(4):337-43. PubMed ID: 7888135
[TBL] [Abstract][Full Text] [Related]
7. Dandy-Walker variant malformation, spastic paraplegia, and mental retardation in two sibs.
Stoll C; Huber C; Alembik Y; Terrade E; Maitrot D
Am J Med Genet; 1990 Sep; 37(1):124-7. PubMed ID: 2240029
[TBL] [Abstract][Full Text] [Related]
8. Short stature, mental retardation and multiple dysmorphisms in two unrelated females: one or two different syndromes or none?
Pfeiffer RA; Kapferer L; Tietze HU
Genet Couns; 1996; 7(3):213-7. PubMed ID: 8897043
[TBL] [Abstract][Full Text] [Related]
9. [Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?].
Sengers RC; Hamel BC; Otten BJ; van Gils JF; de Pagter AG
Tijdschr Kindergeneeskd; 1985 Feb; 53(1):31-4. PubMed ID: 4039476
[TBL] [Abstract][Full Text] [Related]
10. Dandy-Walker malformation in two calves.
Jeffrey M; Preece BE; Holliman A
Vet Rec; 1990 May; 126(20):499-501. PubMed ID: 2368274
[TBL] [Abstract][Full Text] [Related]
11. Ultrasound diagnosis of Dandy-Walker cyst.
Tritrakarn A; Khanjanasthiti P; Bhoopat W
J Med Assoc Thai; 1989 Jan; 72(1):52-5. PubMed ID: 2656899
[TBL] [Abstract][Full Text] [Related]
12. A new X-linked mental retardation syndrome.
Atkin JF; Flaitz K; Patil S; Smith W
Am J Med Genet; 1985 Aug; 21(4):697-705. PubMed ID: 4025397
[TBL] [Abstract][Full Text] [Related]
13. Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
Mégarbané A; Abi Moussa M
Genet Couns; 1997; 8(2):127-32. PubMed ID: 9219011
[TBL] [Abstract][Full Text] [Related]
14. Dandy-Walker malformation with postaxial polydactyly: a new syndrome?
Pierquin G; Deroover J; Levi S; Masson T; Hayez-Delatte F; Van Regemorter N
Am J Med Genet; 1989 Aug; 33(4):483-4. PubMed ID: 2596509
[TBL] [Abstract][Full Text] [Related]
15. A family with three recessive traits and homozygosity for a long 9qh+ chromosome segment.
Christian JC; Dexter RN; Palmer CG; Muller J
Am J Med Genet; 1980; 6(4):301-8. PubMed ID: 6938130
[TBL] [Abstract][Full Text] [Related]
16. Neuropathological analysis of an asymptomatic adult case with Dandy-Walker variant.
Notaridis G; Ebbing K; Giannakopoulos P; Bouras C; Kövari E
Neuropathol Appl Neurobiol; 2006 Jun; 32(3):344-50. PubMed ID: 16640653
[TBL] [Abstract][Full Text] [Related]
17. Ultrasonic evaluation of the Dandy-Walker syndrome.
Kirkinen P; Jouppila P; Valkeakari T; Saukkonen AL
Obstet Gynecol; 1982 Jun; 59(6 Suppl):18S-21S. PubMed ID: 7088419
[TBL] [Abstract][Full Text] [Related]
18. Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.
Ben Hamouda H; Sfar MN; Braham R; Ben Salah M; Ayadi A; Soua H; Hamza H; Sfar MT
Acta Orthop Belg; 2001 Dec; 67(5):528-32. PubMed ID: 11822087
[TBL] [Abstract][Full Text] [Related]
19. Usher syndrome associated with a variant of Dandy-Walker malformation.
Simsek T; Ozdamar Y; Simsek E; Men G
J Pediatr Ophthalmol Strabismus; 2010 May; 47 Online():e1-4. PubMed ID: 21214164
[TBL] [Abstract][Full Text] [Related]
20. [A case of Dandy-Walker malformation. Diagnosis and monitoring using transfontanelle echotomography].
Allard D; Lauras B; Brunon J; Rubet A
Pediatrie; 1982; 37(3):201-5. PubMed ID: 7122182
[No Abstract] [Full Text] [Related]
[Next] [New Search]
