These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

88 related articles for article (PubMed ID: 22431914)

  • 1. Aprosencephaly with otocephaly in a lamb (Ovis aries).
    Brachthäuser L; Klumpp S; Hecht W; Kuchelmeister K; Reinacher M; Ebbert W; Herden C
    Vet Pathol; 2012 Nov; 49(6):1043-8. PubMed ID: 22431914
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. A novel mutation of orthodenticle homeobox 2 contributing to a case of otocephaly initially diagnosed by prenatal ultrasound in the first trimester.
    Jones M; Chung J; Kimonis V; Gold JA
    Clin Dysmorphol; 2017 Apr; 26(2):98-100. PubMed ID: 27442045
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Otx2 and Otx1 protect diencephalon and mesencephalon from caudalization into metencephalon during early brain regionalization.
    Sakurai Y; Kurokawa D; Kiyonari H; Kajikawa E; Suda Y; Aizawa S
    Dev Biol; 2010 Nov; 347(2):392-403. PubMed ID: 20816794
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Atelencephalic aprosencephaly.
    Harris CP; Townsend JJ; Norman MG; White VA; Viskochil DH; Pysher TJ; Klatt EC
    J Child Neurol; 1994 Oct; 9(4):412-6. PubMed ID: 7822735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. External and computed tomography analysis of a strophocephalic lamb.
    Lejong M; Vanmuylder N; Louryan S
    Morphologie; 2019 Jun; 103(341 Pt 2):122-125. PubMed ID: 30853367
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Skeletal dysplasia with craniofacial deformity and disproportionate dwarfism in hair sheep of northeastern Brazil.
    Dantas FP; Medeiros GX; Figueiredo AP; Thompson K; Riet-Correa F
    J Comp Pathol; 2014; 150(2-3):245-52. PubMed ID: 24447571
    [TBL] [Abstract][Full Text] [Related]  

  • 13. XK aprosencephaly and anencephaly in sibs.
    Townes PL; Reuter K; Rosquete EE; Magee BD
    Am J Med Genet; 1988 Mar; 29(3):523-8. PubMed ID: 3287923
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The homeobox gene Otx2 in development and disease.
    Beby F; Lamonerie T
    Exp Eye Res; 2013 Jun; 111():9-16. PubMed ID: 23523800
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Ovine craniofacial malformation: a morphometrical study.
    Eriksen T; Kuiper H; Pielmeier R; Ganter M; Distl O; Staszyk C
    Res Vet Sci; 2012 Dec; 93(3):1122-7. PubMed ID: 22541645
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neonate with meroacrania: radiological findings and review of the literature.
    Yildirim H; Koç M; Kurt N; Artaş H; Aygün D
    Diagn Interv Radiol; 2009 Dec; 15(4):232-5. PubMed ID: 19908184
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Anencephaly in sheep.
    Dennis SM; Leipold HW
    Cornell Vet; 1972 Apr; 62(2):273-81. PubMed ID: 5023994
    [No Abstract]   [Full Text] [Related]  

  • 19. Otx2 cell-autonomously determines dorsal mesencephalon versus cerebellum fate independently of isthmic organizing activity.
    Di Giovannantonio LG; Di Salvio M; Omodei D; Prakash N; Wurst W; Pierani A; Acampora D; Simeone A
    Development; 2014 Jan; 141(2):377-88. PubMed ID: 24335253
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging.
    Chen CP; Wang KG; Huang JK; Chang TY; Lin YH; Chin DT; Tzen CY; Wang W
    Ultrasound Obstet Gynecol; 2003 Aug; 22(2):214-5. PubMed ID: 12905522
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.