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 *

165 related articles for article (PubMed ID: 3372784)

  • 21. Setleis syndrome: genetic and clinical findings in a new case with epilepsy.
    Giordano L; Desnick RJ; Molinaro A; Uliana V; Forzano F; Edelmann L; Nazarenko I; Pinelli L; Accorsi P; Faravelli F
    Pediatr Neurol; 2014 Apr; 50(4):389-91. PubMed ID: 24486222
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A huge absence of skin on the trunk: aplasia cutis congenita.
    Dogan P; Varal IG
    Pan Afr Med J; 2018; 31():234. PubMed ID: 31447991
    [No Abstract]   [Full Text] [Related]  

  • 23. Frequent Occurrence of Aplasia Cutis Congenita in Bullous Dermolysis of the Newborn.
    Diociaiuti A; Castiglia D; Giancristoforo S; Guerra L; Proto V; Dotta A; Boldrini R; Zambruno G; El Hachem M
    Acta Derm Venereol; 2016 Aug; 96(6):784-7. PubMed ID: 26864810
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III).
    Weaver DD; Norby AR; Rosenfeld JA; Proud VK; Spangler BE; Ming JE; Chisholm E; Zackai EH; Lee BH; Edelmann L; Desnick RJ
    Am J Med Genet A; 2015 May; 167A(5):1061-70. PubMed ID: 25728400
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bullous aplasia cutis congenita.
    Colon-Fontanez F; Fallon Friedlander S; Newbury R; Eichenfield LF
    J Am Acad Dermatol; 2003 May; 48(5 Suppl):S95-8. PubMed ID: 12734490
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epilepsy in a patient with focal dermal hypoplasia.
    Kanemura H; Hatakeyama K; Sugita K; Aihara M
    Pediatr Neurol; 2011 Feb; 44(2):135-8. PubMed ID: 21215914
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Aplasia cutis congenita--a case study of a family with two siblings with this disorder.
    Anderson SM
    S D Med; 2013 Feb; 66(2):48-50. PubMed ID: 23513358
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Aplasia cutis congenita in a defined population from northwest Spain.
    Martinez-Regueira S; Vazquez-Lopez ME; Somoza-Rubio C; Morales-Redondo R; Gonzalez-Gay MA
    Pediatr Dermatol; 2006; 23(6):528-32. PubMed ID: 17155992
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The focal facial dermal dysplasias: phenotypic spectrum and molecular genetic heterogeneity.
    Lee BH; Aggarwal A; Slavotinek A; Edelmann L; Chen B; Desnick RJ
    J Med Genet; 2017 Sep; 54(9):585-590. PubMed ID: 28663233
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Focal dermal hypoplasia syndrome in the neonate.
    Lawlor F; Holmes SC
    J R Soc Med; 1989 Mar; 82(3):165-6. PubMed ID: 2704015
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. A rare case of aplasia cutis congenita.
    Dahmardehei M
    Acta Med Iran; 2013 May; 51(5):341-4. PubMed ID: 23737321
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Goltz-Gorlin syndrome without focal dermal hypoplasia].
    van der Kerkhof PC; Perret CM; Happle R
    Hautarzt; 1988 Nov; 39(11):743-5. PubMed ID: 3243717
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Focal dermal hypoplasia (Goltz syndrome)].
    Corona-Guerra GX; Ochoa-Apreza M
    Bol Med Hosp Infant Mex; 2018; 75(3):178-182. PubMed ID: 29799531
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Phenotypic and molecular characterization of focal dermal hypoplasia in 18 individuals.
    Bostwick B; Fang P; Patel A; Sutton VR
    Am J Med Genet C Semin Med Genet; 2016 Mar; 172C(1):9-20. PubMed ID: 26853229
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Electronmicroscopic observation of the basement membrane zone in focal dermal hypoplasia.
    Lee IJ; Cha MS; Kim SC; Bang D
    Pediatr Dermatol; 1996; 13(1):5-9. PubMed ID: 8919515
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dermatologic findings of focal dermal hypoplasia (Goltz syndrome).
    Bree AF; Grange DK; Hicks MJ; Goltz RW
    Am J Med Genet C Semin Med Genet; 2016 Mar; 172C(1):44-51. PubMed ID: 26858134
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Aplasia cutis congenita of the trunk with fetus papyraceus.
    Kelly BJ; Samolitis NJ; Xie DL; Skidmore RA
    Pediatr Dermatol; 2002; 19(4):326-9. PubMed ID: 12220278
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. [Meso-ectodermal polydysplasia with focal dermal hypoplasia: on a case of Goltz syndrome].
    Patrizi A; Pizzino D; Varotti C
    G Ital Dermatol Venereol; 1987 May; 122(5):251-4. PubMed ID: 3623619
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.