53 related articles for article (PubMed ID: 17593378)
1. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
Aykut A; Cogulu O; Ekmekci AY; Ozkinay F
Genet Couns; 2008; 19(2):237-40. PubMed ID: 18618999
[TBL] [Abstract][Full Text] [Related]
2. [The acrocallosal syndrome. Report of an additional case].
Wendisch J; Lorenz P; Kabus M; Rupprecht E; Walther S
Kinderarztl Prax; 1990 Jun; 58(6):315-21. PubMed ID: 2166860
[TBL] [Abstract][Full Text] [Related]
3. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
Marafie MJ; Temtamy SA; Rajaram U; al-Awadi SA; el-Badramany MH; Farag TI
Am J Med Genet; 1996 Dec; 66(3):261-4. PubMed ID: 8985483
[TBL] [Abstract][Full Text] [Related]
4. Acrocallosal syndrome in fetus: focus on additional brain abnormalities.
Fernandez C; Soulier M; Coulibaly B; Liprandi A; Benoit B; Giuliano F; Sigaudy S; Figarella-Branger D; Fallet-Bianco C
Acta Neuropathol; 2008 Jan; 115(1):151-6. PubMed ID: 17593378
[TBL] [Abstract][Full Text] [Related]
5. Hypogenitalism in the acrocallosal syndrome.
Temtamy SA; Meguid NA
Am J Med Genet; 1989 Mar; 32(3):301-5. PubMed ID: 2658583
[TBL] [Abstract][Full Text] [Related]
6. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
Jonas RE; Kimonis VE; Morales A
Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
[TBL] [Abstract][Full Text] [Related]
7. Acrocallosal syndrome: additional manifestations.
Casamassima AC; Beneck D; Gewitz MH; Horowitz MA; Woolf PK; Pettersen IM; Shapiro LR
Am J Med Genet; 1989 Mar; 32(3):311-7. PubMed ID: 2658584
[TBL] [Abstract][Full Text] [Related]
8. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
9. [Renal hypoplasia, polydactyly, cardiopathy: a new syndrome?].
Bonnet J; Cordier MP; Ollagnon E; Guillaud MH; Raudrant D; Robert JM; Charvet F
J Genet Hum; 1987 Aug; 35(4):279-89. PubMed ID: 3309184
[TBL] [Abstract][Full Text] [Related]
10. Fryns syndrome survivors and neurologic outcome.
Van Hove JL; Spiridigliozzi GA; Heinz R; McConkie-Rosell A; Iafolla AK; Kahler SG
Am J Med Genet; 1995 Nov; 59(3):334-40. PubMed ID: 8599357
[TBL] [Abstract][Full Text] [Related]
11.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]