24 related articles for article (PubMed ID: 12575660)
1. The Greig cephalopolysyndactyly syndrome.
Biesecker LG
Orphanet J Rare Dis; 2008 Apr; 3():10. PubMed ID: 18435847
[TBL] [Abstract][Full Text] [Related]
2. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
Johnston JJ; Olivos-Glander I; Killoran C; Elson E; Turner JT; Peters KF; Abbott MH; Aughton DJ; Aylsworth AS; Bamshad MJ; Booth C; Curry CJ; David A; Dinulos MB; Flannery DB; Fox MA; Graham JM; Grange DK; Guttmacher AE; Hannibal MC; Henn W; Hennekam RC; Holmes LB; Hoyme HE; Leppig KA; Lin AE; Macleod P; Manchester DK; Marcelis C; Mazzanti L; McCann E; McDonald MT; Mendelsohn NJ; Moeschler JB; Moghaddam B; Neri G; Newbury-Ecob R; Pagon RA; Phillips JA; Sadler LS; Stoler JM; Tilstra D; Walsh Vockley CM; Zackai EH; Zadeh TM; Brueton L; Black GC; Biesecker LG
Am J Hum Genet; 2005 Apr; 76(4):609-22. PubMed ID: 15739154
[TBL] [Abstract][Full Text] [Related]
3. A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene.
Hui CC; Joyner AL
Nat Genet; 1993 Mar; 3(3):241-6. PubMed ID: 8387379
[TBL] [Abstract][Full Text] [Related]
4. Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.
Williams PG; Hersh JH; Yen FF; Barch MJ; Kleinert HE; Kunz J; Kalff-Suske M
Clin Genet; 1997 Dec; 52(6):436-41. PubMed ID: 9520255
[TBL] [Abstract][Full Text] [Related]
5. Point mutations in human GLI3 cause Greig syndrome.
Wild A; Kalff-Suske M; Vortkamp A; Bornholdt D; König R; Grzeschik KH
Hum Mol Genet; 1997 Oct; 6(11):1979-84. PubMed ID: 9302279
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigation.
Bilguvar K; Bydon M; Bayrakli F; Ercan-Sencicek AG; Bayri Y; Mason C; DiLuna ML; Seashore M; Bronen R; Lifton RP; State M; Gunel M
J Neurosurg; 2007 Dec; 107(6 Suppl):495-9. PubMed ID: 18154020
[TBL] [Abstract][Full Text] [Related]
8. Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome.
Driess S; Freese K; Bornholdt D; Kobelt A; Kress W; Mortier G; Radhakrishna U; Antonarakis SE; Rauch A; Suri M; Verheij JB; Woerle H; Grzeschik KH; Kalff-Suske M
Hum Genet; 2003 Jan; 112(1):103. PubMed ID: 12575660
[No Abstract] [Full Text] [Related]
9. [Greig cephalopolysyndactyly syndrome].
Satokata I
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):184-6. PubMed ID: 11057189
[No Abstract] [Full Text] [Related]
10. Central nervous system abnormalities in oculodentodigital dysplasia.
Schrander-Stumpel CT; Franke CL
Genet Couns; 1996; 7(3):233-5. PubMed ID: 8897047
[No Abstract] [Full Text] [Related]
11. [Polysyndactyly-dysmorphic craniofacies, Greig type].
Numabe H
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):522-3. PubMed ID: 11528873
[No Abstract] [Full Text] [Related]
12. [Nijmegen breakage syndrome].
Matsuura S
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):320-2. PubMed ID: 11528761
[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]
