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 *

190 related articles for article (PubMed ID: 1173820)

  • 1. The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs.
    Scribanu N; Temtamy SA
    J Pediatr; 1975 Jul; 87(1):79-82. PubMed ID: 1173820
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome.
    Bilginer B; Onal MB; Bahadir S; Akalan N
    Turk Neurosurg; 2008 Apr; 18(2):191-3. PubMed ID: 18597236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Homozygosity for a novel DOCK6 variant in an individual without aplasia cutis congenita of the scalp and terminal transverse limb defects.
    Zaersabet M; Koochakkhani S; Sarmast Y; Salmani H
    Clin Dysmorphol; 2023 Apr; 32(2):84-87. PubMed ID: 36779775
    [No Abstract]   [Full Text] [Related]  

  • 6. Adams-Oliver syndrome.
    Iftikhar N; Ahmad Ghumman FI; Janjua SA; Ejaz A; Butt UA
    J Coll Physicians Surg Pak; 2014 May; 24 Suppl 2():S76-7. PubMed ID: 24906278
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome?
    Toriello HV; Graff RG; Florentine MF; Lacina S; Moore WD
    Am J Med Genet; 1988 Feb; 29(2):269-76. PubMed ID: 3354598
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Our experience with a severe case of aplasia cutis congenita with a large skull defect.
    Puvabanditsin S; February M; Garrow E; Bruno C; Mehta R
    Int J Dermatol; 2016 Oct; 55(10):1151-3. PubMed ID: 26228315
    [No Abstract]   [Full Text] [Related]  

  • 9. Terminal transverse defects with aplasia cutis congenita (Adams-Oliver syndrome).
    Shapiro SD; Escobedo MK
    Birth Defects Orig Artic Ser; 1985; 21(2):135-42. PubMed ID: 4041576
    [No Abstract]   [Full Text] [Related]  

  • 10. Aplasia cutis congenita in a CDC42-related developmental phenotype.
    Schnabel F; Kamphausen SB; Funke R; Kaulfuß S; Wollnik B; Zenker M
    Am J Med Genet A; 2021 Mar; 185(3):850-855. PubMed ID: 33283961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome.
    Khashab ME; Rhee ST; Pierce SD; Khashab YE; Nejat F; Fried A
    J Neurosurg Pediatr; 2009 Dec; 4(6):523-7. PubMed ID: 19951037
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aplasia cutis congenita: a clinical review and associated defects.
    Blunt K; Quan V; Carr D; Paes BA
    Neonatal Netw; 1992 Oct; 11(7):17-27. PubMed ID: 1406547
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.
    Snape KM; Ruddy D; Zenker M; Wuyts W; Whiteford M; Johnson D; Lam W; Trembath RC
    Am J Med Genet A; 2009 Aug; 149A(8):1860-81. PubMed ID: 19610107
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
    Caksen H; Kurtoğlu S
    Acta Neurol Belg; 2000 Dec; 100(4):252-5. PubMed ID: 11233683
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: a possible link to the Adams-Oliver syndrome.
    Digilio MC; Marino B; Dallapiccola B
    Am J Med Genet A; 2008 Nov; 146A(21):2842-4. PubMed ID: 18924173
    [No Abstract]   [Full Text] [Related]  

  • 17. Adams-Oliver syndrome revisited.
    Whitley CB; Gorlin RJ
    Am J Med Genet; 1991 Sep; 40(3):319-26. PubMed ID: 1951437
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aplasia cutis congenita, terminal limb defects and falciform retinal folds: confirmation of a distinct syndrome of vascular disruption.
    Prothero J; Nicholl R; Wilson J; Wakeling EL
    Clin Dysmorphol; 2007 Jan; 16(1):39-41. PubMed ID: 17159513
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A case of extensive aplasia cutis congenita: a conservative approach.
    Starcevic M; Sepec MP; Zah V
    Pediatr Dermatol; 2010; 27(5):540-2. PubMed ID: 20807357
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.