102 related articles for article (PubMed ID: 21345367)
1. In silico identification of new candidate genes for hereditary congenital facial paresis.
Tomás-Roca L; Pérez-Aytés A; Puelles L; Marín F
Int J Dev Neurosci; 2011 Jun; 29(4):451-60. PubMed ID: 21345367
[TBL] [Abstract][Full Text] [Related]
2. Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes.
Michielse CB; Bhat M; Brady A; Jafrid H; van den Hurk JA; Raashid Y; Brunner HG; van Bokhoven H; Padberg GW
Eur J Hum Genet; 2006 Dec; 14(12):1306-12. PubMed ID: 16912702
[TBL] [Abstract][Full Text] [Related]
3. Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis.
Vogel M; Velleuer E; Schmidt-Jiménez LF; Mayatepek E; Borkhardt A; Alawi M; Kutsche K; Kortüm F
Am J Med Genet A; 2016 Jul; 170(7):1813-9. PubMed ID: 27144914
[TBL] [Abstract][Full Text] [Related]
4. Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouse.
van der Zwaag B; Burbach JP; Scharfe C; Oefner PJ; Brunner HG; Padberg GW; van Bokhoven H
Genomics; 2005 Jul; 86(1):55-67. PubMed ID: 15953540
[TBL] [Abstract][Full Text] [Related]
5. Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.
van der Zwaag B; Burbach JP; Brunner HG; van Bokhoven H; Padberg GW
Brain Res Dev Brain Res; 2005 Aug; 158(1-2):66-71. PubMed ID: 15996756
[TBL] [Abstract][Full Text] [Related]
6. Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP; Di Gioia SA; Webb BD; Chan WM; de Boer E; Garnai SJ; Barry BJ; Ray T; Kosicki M; Robson CD; Zhang Z; Collins TE; Gelber A; Pratt BM; Fujiwara Y; Varshney A; Lek M; Warburton PE; Van Ryzin C; Lehky TJ; Zalewski C; King KA; Brewer CC; Thurm A; Snow J; Facio FM; Narisu N; Bonnycastle LL; Swift A; Chines PS; Bell JL; Mohan S; Whitman MC; Staffieri SE; Elder JE; Demer JL; Torres A; Rachid E; Al-Haddad C; Boustany RM; Mackey DA; Brady AF; Fenollar-Cortés M; Fradin M; Kleefstra T; Padberg GW; Raskin S; Sato MT; Orkin SH; Parker SCJ; Hadlock TA; Vissers LELM; van Bokhoven H; Jabs EW; Collins FS; Pennacchio LA; Manoli I; Engle EC
Nat Genet; 2023 Jul; 55(7):1149-1163. PubMed ID: 37386251
[TBL] [Abstract][Full Text] [Related]
7. A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.
Sahin Y; Güngör O; Ayaz A; Güngör G; Sahin B; Yaykasli K; Ceylaner S
Brain Dev; 2017 Feb; 39(2):166-170. PubMed ID: 27640920
[TBL] [Abstract][Full Text] [Related]
8. A family with hereditary congenital facial paresis and a brief review of the literature.
Alrashdi IS; Rich P; Patton MA
Clin Dysmorphol; 2010 Oct; 19(4):198-201. PubMed ID: 20577083
[TBL] [Abstract][Full Text] [Related]
9. Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family.
Kremer H; Kuyt LP; van den Helm B; van Reen M; Leunissen JA; Hamel BC; Jansen C; Mariman EC; Frants RR; Padberg GW
Hum Mol Genet; 1996 Sep; 5(9):1367-71. PubMed ID: 8872479
[TBL] [Abstract][Full Text] [Related]
10. A new hereditary congenital facial palsy case supports arg5 in HOX-DNA binding domain as possible hot spot for mutations.
Uyguner ZO; Toksoy G; Altunoglu U; Ozgur H; Basaran S; Kayserili H
Eur J Med Genet; 2015; 58(6-7):358-63. PubMed ID: 26007620
[TBL] [Abstract][Full Text] [Related]
11. LIFR beta plays a major role in neuronal identity determination and glial differentiation in the mouse facial nucleus.
Alfonsi F; Filippi P; Salaun D; deLapeyrière O; Durbec P
Dev Biol; 2008 Jan; 313(1):267-78. PubMed ID: 18031722
[TBL] [Abstract][Full Text] [Related]
12. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
13. Hereditary congenital facial paralysis.
Nicolai JP; Bos MY; ter Haar BG
Scand J Plast Reconstr Surg; 1986; 20(1):37-9. PubMed ID: 3775291
[TBL] [Abstract][Full Text] [Related]
14. The murine DSCR1-like (Down syndrome candidate region 1) gene family: conserved synteny with the human orthologous genes.
Strippoli P; Petrini M; Lenzi L; Carinci P; Zannotti M
Gene; 2000 Oct; 257(2):223-32. PubMed ID: 11080588
[TBL] [Abstract][Full Text] [Related]
15. Congenital hereditary paresis of ramus marginalis nervus facialis in five generations.
Hölmich LR; Medgyesi S
Ann Plast Surg; 1994 Jul; 33(1):96-9. PubMed ID: 7944209
[TBL] [Abstract][Full Text] [Related]
16. [Congenital central paralysis of the facial nerve in a newborn infant].
Rudelić I; Zuzek A; Druzetić K; Rudelić E
Jugosl Ginekol Opstet; 1983; 23(1-2):37-40. PubMed ID: 6645616
[TBL] [Abstract][Full Text] [Related]
17. The congenital cranial dysinnervation disorders.
Gutowski NJ; Chilton JK
Arch Dis Child; 2015 Jul; 100(7):678-81. PubMed ID: 25633065
[TBL] [Abstract][Full Text] [Related]
18. The atypical cadherin Celsr1 functions non-cell autonomously to block rostral migration of facial branchiomotor neurons in mice.
Glasco DM; Pike W; Qu Y; Reustle L; Misra K; Di Bonito M; Studer M; Fritzsch B; Goffinet AM; Tissir F; Chandrasekhar A
Dev Biol; 2016 Sep; 417(1):40-9. PubMed ID: 27395006
[TBL] [Abstract][Full Text] [Related]
19. Homeo box gene complex on mouse chromosome 11: molecular cloning, expression in embryogenesis, and homology to a human homeo box locus.
Hart CP; Awgulewitsch A; Fainsod A; McGinnis W; Ruddle FH
Cell; 1985 Nov; 43(1):9-18. PubMed ID: 3000607
[TBL] [Abstract][Full Text] [Related]
20. Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3.
Murtazina A; Borovikov A; Kuchina A; Ovsova O; Bulakh M; Chukhrova A; Braslavskaya S; Ryzhkova O; Skryabin N; Kutsev S; Dadali E
Int J Mol Sci; 2023 Dec; 25(1):. PubMed ID: 38203298
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]