141 related articles for article (PubMed ID: 24167467)
1. Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2.
Patat O; van Ravenswaaij-Arts CM; Tantau J; Corsten-Janssen N; van Tintelen JP; Dijkhuizen T; Kaplan J; Chassaing N
Mol Syndromol; 2013 Sep; 4(6):302-5. PubMed ID: 24167467
[TBL] [Abstract][Full Text] [Related]
2. Re-focusing on Agnathia-Otocephaly complex.
Dubucs C; Chassaing N; Sergi C; Aubert-Mucca M; Attié-Bitach T; Lacombe D; Thauvin-Robinet C; Arpin S; Perez MJ; Cabrol C; Chen CP; Aziza J; Colin E; Martinovic J; Calvas P; Plaisancié J
Clin Oral Investig; 2021 Mar; 25(3):1353-1362. PubMed ID: 32643087
[TBL] [Abstract][Full Text] [Related]
3. OTX2 mutations contribute to the otocephaly-dysgnathia complex.
Chassaing N; Sorrentino S; Davis EE; Martin-Coignard D; Iacovelli A; Paznekas W; Webb BD; Faye-Petersen O; Encha-Razavi F; Lequeux L; Vigouroux A; Yesilyurt A; Boyadjiev SA; Kayserili H; Loget P; Carles D; Sergi C; Puvabanditsin S; Chen CP; Etchevers HC; Katsanis N; Mercer CL; Calvas P; Jabs EW
J Med Genet; 2012 Jun; 49(6):373-9. PubMed ID: 22577225
[TBL] [Abstract][Full Text] [Related]
4. Agnathia-otocephaly complex: a case report and examination of the OTX2 and PRRX1 genes.
Herman S; Delio M; Morrow B; Samanich J
Gene; 2012 Feb; 494(1):124-9. PubMed ID: 22198066
[TBL] [Abstract][Full Text] [Related]
5. Agnathia-Otocephaly Complex Due to a De Novo Deletion in the
Fabiani M; Libotte F; Margiotti K; Tannous DKI; Sparacino D; D'Aleo MP; Monaco F; Dello Russo C; Mesoraca A; Giorlandino C
Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553536
[TBL] [Abstract][Full Text] [Related]
6. Agnathia-otocephaly complex and asymmetric velopharyngeal insufficiency due to an in-frame duplication in OTX2.
Sergouniotis PI; Urquhart JE; Williams SG; Bhaskar SS; Black GC; Lovell SC; Whitby DJ; Newman WG; Clayton-Smith J
J Hum Genet; 2015 Apr; 60(4):199-202. PubMed ID: 25589041
[TBL] [Abstract][Full Text] [Related]
7. A de novo variant in OTX2 in a lamb with otocephaly.
Paris JM; Letko A; Häfliger IM; Švara T; Gombač M; Klinc P; Škibin A; Pogorevc E; Drögemüller C
Acta Vet Scand; 2020 Jan; 62(1):5. PubMed ID: 31969185
[TBL] [Abstract][Full Text] [Related]
8. Expanding the spectrum of SMAD3-related phenotypes to agnathia-otocephaly.
Meier N; Bruder E; Miny P; Tercanli S; Filges I
Mol Genet Genomic Med; 2020 Apr; 8(4):e1178. PubMed ID: 32100971
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis and molecular genetic studies on a new case of agnathia-otocephaly.
Kamnasaran D; Morin F; Gekas J
Fetal Pediatr Pathol; 2010; 29(4):207-11. PubMed ID: 20594144
[TBL] [Abstract][Full Text] [Related]
10. Genetic modifiers of otocephalic phenotypes in Otx2 heterozygous mutant mice.
Hide T; Hatakeyama J; Kimura-Yoshida C; Tian E; Takeda N; Ushio Y; Shiroishi T; Aizawa S; Matsuo I
Development; 2002 Sep; 129(18):4347-57. PubMed ID: 12183386
[TBL] [Abstract][Full Text] [Related]
11. Agnathia otocephaly: A case from the Katanga Copperbelt.
Kayembe-Kitenge T; Manyong'a Kadiamba V; de Luca C; Musa Obadia P; Kasamba Ilunga E; Mbuyi-Musanzayi S; Nawrot T; Lubaba Nkulu CB; Nemery B; Devriendt K
Birth Defects Res; 2020 Oct; 112(16):1287-1291. PubMed ID: 32639113
[TBL] [Abstract][Full Text] [Related]
12. Prenatal Diagnosis of Otocephaly: A Rare Facial Anomaly.
Goenka S; Sahithi K; Ratha C
J Obstet Gynaecol India; 2022 Aug; 72(4):364-368. PubMed ID: 35923505
[TBL] [Abstract][Full Text] [Related]
13. Computed tomographic reconstruction of a fetus with the dysgnathia complex (agnathia-otocephaly).
Rajan PV; Wing DA; Bocian M; McKeown A
Prenat Diagn; 2007 Feb; 27(2):130-2. PubMed ID: 17152114
[TBL] [Abstract][Full Text] [Related]
14. Current perspectives on the etiology of agnathia-otocephaly.
Gekas J; Li B; Kamnasaran D
Eur J Med Genet; 2010; 53(6):358-66. PubMed ID: 20849990
[TBL] [Abstract][Full Text] [Related]
15. Cyclopia: isolated and with agnathia-otocephaly complex.
Wai LT; Chandran S
BMJ Case Rep; 2017 Aug; 2017():. PubMed ID: 28855214
[TBL] [Abstract][Full Text] [Related]
16. Mandibular dysostosis without microphthalmia caused by OTX2 deletion.
Latypova X; Bordereau S; Bleriot A; Pichon O; Poulain D; Briand A; Le Caignec C; Isidor B
Am J Med Genet A; 2016 Sep; 170(9):2466-70. PubMed ID: 27378064
[TBL] [Abstract][Full Text] [Related]
17. Severe Agnathia-Otocephaly Complex: Surgical Management and Longitudinal Follow-up From Birth Through Adulthood.
Golinko MS; Shetye P; Flores RL; Staffenberg DA
J Craniofac Surg; 2015 Nov; 26(8):2387-92. PubMed ID: 26517463
[TBL] [Abstract][Full Text] [Related]
18. Recurrent agnathia-otocephaly caused by DNA replication slippage in PRRX1.
Dasouki M; Andrews B; Parimi P; Kamnasaran D
Am J Med Genet A; 2013 Apr; 161A(4):803-8. PubMed ID: 23444262
[TBL] [Abstract][Full Text] [Related]
19. Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype.
Dateki S; Kosaka K; Hasegawa K; Tanaka H; Azuma N; Yokoya S; Muroya K; Adachi M; Tajima T; Motomura K; Kinoshita E; Moriuchi H; Sato N; Fukami M; Ogata T
J Clin Endocrinol Metab; 2010 Feb; 95(2):756-64. PubMed ID: 19965921
[TBL] [Abstract][Full Text] [Related]
20. Otocephaly: Agnathia- Microstomia-Synotia Syndrome- A Rare Congenital Anomaly.
Jagtap SV; Saini N; Jagtap S; Saini S
J Clin Diagn Res; 2015 Sep; 9(9):ED03-4. PubMed ID: 26500912
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
