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 *

285 related articles for article (PubMed ID: 21978514)

  • 21. 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]  

  • 22. Intracranial Calcifications in Young Children.
    Dugan SL; Botto LD; Hedlund GL; Bale JF
    Semin Pediatr Neurol; 2018 Jul; 26():135-139. PubMed ID: 29961505
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The developmental biology of genetic Notch disorders.
    Mašek J; Andersson ER
    Development; 2017 May; 144(10):1743-1763. PubMed ID: 28512196
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Adams-Oliver syndrome associated with refractory glaucoma.
    Pillai MR; Pabolu C; R R; Chaudhary S; Sr K; Puthuran GV
    J AAPOS; 2024 Aug; 28(4):103950. PubMed ID: 38866321
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Aplasia cutis congenita: approach to evaluation and management.
    Browning JC
    Dermatol Ther; 2013; 26(6):439-44. PubMed ID: 24552406
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Adams Oliver syndrome in association with neurological deficit.
    Brar BK; Mahajan BB; Puri N
    Eur J Dermatol; 2010; 20(3):413-4. PubMed ID: 20406727
    [No Abstract]   [Full Text] [Related]  

  • 29. Septo-optic dysplasia, limb anomalies and cutis aplasia: further evidence for overlap between Pagon and Adams-Oliver syndromes.
    Pottinger CC; Joshi H; Rowe SA; Fryer AE
    Clin Dysmorphol; 2009 Oct; 18(4):228-31. PubMed ID: 19623038
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. [The Adams-Oliver syndrome in Spain: the epidemiological aspects].
    Martínez-Frías ML; Arroyo Carrera I; Muñoz-Delgado NJ; Nieto Conde C; Rodríguez-Pinilla E; Urioste Azcorra M; Omeñaca Teres F; García Alix A
    An Esp Pediatr; 1996 Jul; 45(1):57-61. PubMed ID: 8849132
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Unique variant of Adams-Oliver syndrome with dilated cardiomyopathy and heart block.
    Atasoy HI; Tug E; Yavuz T; Cine N
    Pediatr Int; 2013 Aug; 55(4):508-12. PubMed ID: 23910800
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome.
    Yu X; Wang RR; Han SR; Bai X; Habulieti X; Sun Y; Sun LW; Zhang H; Khan A; Zhang X
    Chin Med J (Engl); 2019 Jul; 132(14):1755-1757. PubMed ID: 31261205
    [No Abstract]   [Full Text] [Related]  

  • 35. 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]  

  • 36. Expanding the phenotype in Adams-Oliver syndrome correlating with the genotype.
    Dudoignon B; Huber C; Michot C; Di Rocco F; Girard M; Lyonnet S; Rio M; Rabia SH; Daire VC; Baujat G
    Am J Med Genet A; 2020 Jan; 182(1):29-37. PubMed ID: 31654484
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Adams-Oliver syndrome associated with bilateral anterior polar cataracts and optic disk drusen.
    Lascaratos G; Lam WW; Newman WD; MacRae M
    J AAPOS; 2011 Jun; 15(3):299-301. PubMed ID: 21641251
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.
    Meester JA; Southgate L; Stittrich AB; Venselaar H; Beekmans SJ; den Hollander N; Bijlsma EK; Helderman-van den Enden A; Verheij JB; Glusman G; Roach JC; Lehman A; Patel MS; de Vries BB; Ruivenkamp C; Itin P; Prescott K; Clarke S; Trembath R; Zenker M; Sukalo M; Van Laer L; Loeys B; Wuyts W
    Am J Hum Genet; 2015 Sep; 97(3):475-82. PubMed ID: 26299364
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Autosomal recessive Adams-Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase.
    Cohen I; Silberstein E; Perez Y; Landau D; Elbedour K; Langer Y; Kadir R; Volodarsky M; Sivan S; Narkis G; Birk OS
    Eur J Hum Genet; 2014 Mar; 22(3):374-8. PubMed ID: 23860037
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.