151 related articles for article (PubMed ID: 24862819)
1. Severe phenotype in two half-sibs with Adams Oliver syndrome.
Sevilla-Montoya R; Ríos-Flores B; Moreno-Verduzco E; Domínguez-Castro M; Rivera-Pedroza CI; Aguinaga-Ríos DM
Arch Argent Pediatr; 2014 Jun; 112(3):e108-12. PubMed ID: 24862819
[TBL] [Abstract][Full Text] [Related]
2. Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.
Jones KM; Silfvast-Kaiser A; Leake DR; Diaz LZ; Levy ML
Pediatr Dermatol; 2017 Sep; 34(5):e249-e253. PubMed ID: 28884918
[TBL] [Abstract][Full Text] [Related]
3. Adams-Oliver syndrome caused by mutations of the EOGT gene.
Schröder KC; Duman D; Tekin M; Schanze D; Sukalo M; Meester J; Wuyts W; Zenker M
Am J Med Genet A; 2019 Nov; 179(11):2246-2251. PubMed ID: 31368252
[TBL] [Abstract][Full Text] [Related]
4. Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype.
Hassed S; Li S; Mulvihill J; Aston C; Palmer S
Am J Med Genet A; 2017 Mar; 173(3):790-800. PubMed ID: 28160419
[TBL] [Abstract][Full Text] [Related]
5. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies.
Sukalo M; Tilsen F; Kayserili H; Müller D; Tüysüz B; Ruddy DM; Wakeling E; Ørstavik KH; Snape KM; Trembath R; De Smedt M; van der Aa N; Skalej M; Mundlos S; Wuyts W; Southgate L; Zenker M
Hum Mutat; 2015 Jun; 36(6):593-8. PubMed ID: 25824905
[TBL] [Abstract][Full Text] [Related]
6. Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.
Vandersteen AM; Dixon JW
Clin Dysmorphol; 2011 Oct; 20(4):210-213. PubMed ID: 21785343
[No Abstract] [Full Text] [Related]
7. Cutaneous squamous cell carcinoma in an autosomal-recessive Adams-Oliver syndrome patient with a novel frameshift pathogenic variant in the EOGT gene.
Lukas ML; Harald G; Sanz J; Trippel M; Sabina G; Jochen R
Am J Med Genet A; 2022 Nov; 188(11):3318-3323. PubMed ID: 36059114
[TBL] [Abstract][Full Text] [Related]
8. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
Yağci-Küpeli B; Çağlar K; Büyük S; Balci S
Genet Couns; 2011; 22(1):55-61. PubMed ID: 21614989
[TBL] [Abstract][Full Text] [Related]
9. Distal Limb Defects and Aplasia Cutis: Adams-Oliver Syndrome.
Renfree KJ; Dell PC
J Hand Surg Am; 2016 Jul; 41(7):e207-10. PubMed ID: 27178874
[TBL] [Abstract][Full Text] [Related]
10. A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.
Rojnueangnit K; Phawan T; Khetkham T; Techasatid W; Sirichongkolthong B
Am J Med Genet A; 2022 Feb; 188(2):658-664. PubMed ID: 34755929
[TBL] [Abstract][Full Text] [Related]
11. Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
Meester JAN; Sukalo M; Schröder KC; Schanze D; Baynam G; Borck G; Bramswig NC; Duman D; Gilbert-Dussardier B; Holder-Espinasse M; Itin P; Johnson DS; Joss S; Koillinen H; McKenzie F; Morton J; Nelle H; Reardon W; Roll C; Salih MA; Savarirayan R; Scurr I; Splitt M; Thompson E; Titheradge H; Travers CP; Van Maldergem L; Whiteford M; Wieczorek D; Vandeweyer G; Trembath R; Van Laer L; Loeys BL; Zenker M; Southgate L; Wuyts W
Hum Mutat; 2018 Sep; 39(9):1246-1261. PubMed ID: 29924900
[TBL] [Abstract][Full Text] [Related]
12. [Adams-Oliver syndrome: a case with minimal expression].
Messerer M; Diabira S; Belliard H; Hamlat A
Arch Pediatr; 2010 Oct; 17(10):1460-4. PubMed ID: 20728324
[TBL] [Abstract][Full Text] [Related]
13. Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral Phenotype.
Pisciotta L; Capra V; Accogli A; Giacomini T; Prato G; Tavares P; Pinto-Basto J; Morana G; Mancardi MM
Neuropediatrics; 2018 Jun; 49(3):217-221. PubMed ID: 29631299
[TBL] [Abstract][Full Text] [Related]
14. Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.
Nagasaka M; Taniguchi-Ikeda M; Inagaki H; Ouchi Y; Kurokawa D; Yamana K; Harada R; Nozu K; Sakai Y; Mishra SK; Yamaguchi Y; Morioka I; Toda T; Kurahashi H; Iijima K
J Hum Genet; 2017 Sep; 62(9):851-855. PubMed ID: 28446798
[TBL] [Abstract][Full Text] [Related]
15. A novel variant in DOCK6 gene associated with Adams-Oliver syndrome type 2.
Alzahem T; Alsalamah AK; Mura M; Alsulaiman SM
Ophthalmic Genet; 2020 Aug; 41(4):377-380. PubMed ID: 32498638
[TBL] [Abstract][Full Text] [Related]
16. Adams-Oliver syndrome: a case report.
Frantz JA; Lehmkuhl RL; Leitis LH; Uliano VG; Siementcoski GA
Pediatr Dermatol; 2015; 32(3):383-5. PubMed ID: 25556654
[TBL] [Abstract][Full Text] [Related]
17. Diffuse angiopathy in Adams-Oliver syndrome associated with truncating DOCK6 mutations.
Lehman A; Stittrich AB; Glusman G; Zong Z; Li H; Eydoux P; Senger C; Lyons C; Roach JC; Patel M
Am J Med Genet A; 2014 Oct; 164A(10):2656-62. PubMed ID: 25091416
[TBL] [Abstract][Full Text] [Related]
18. Adams-Oliver syndrome in a newborn infant.
Zakanj Z; Bedek D; Kotrulja L; Ozanic Bulic S
Int J Dermatol; 2016 Feb; 55(2):215-7. PubMed ID: 24697559
[No Abstract] [Full Text] [Related]
19. [Adams-Oliver syndrome and cutis marmorata telangiectatica congenita].
Kojmane W; Hmami F; Atmani S
Ann Dermatol Venereol; 2019 Mar; 146(3):223-225. PubMed ID: 30638685
[TBL] [Abstract][Full Text] [Related]
20. Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutations.
Isrie M; Wuyts W; Van Esch H; Devriendt K
Am J Med Genet A; 2014 Jun; 164A(6):1576-9. PubMed ID: 24668619
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
