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 *

99 related articles for article (PubMed ID: 18616779)

  • 1. Alopecia-mental retardation syndrome: clinical and molecular characterization of four patients.
    Tzschach A; Bozorgmehr B; Hadavi V; Kahrizi K; Garshasbi M; Motazacker MM; Ropers HH; Kuss AW; Najmabadi H
    Br J Dermatol; 2008 Sep; 159(3):748-51. PubMed ID: 18616779
    [No Abstract]   [Full Text] [Related]  

  • 2. Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome.
    Martino F; D'Eufemia P; Pergola MS; Finocchiaro R; Celli M; Giampà G; Frontali M; Giardini O
    Am J Med Genet; 1992 Sep; 44(2):233-6. PubMed ID: 1456297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Neuroectodermosis with alopecia or hypotrichosis. Review of the literature].
    Perniola T; Krajewska G; Carnevale F
    Acta Neurol (Napoli); 1977; 32(3):357-79. PubMed ID: 883530
    [No Abstract]   [Full Text] [Related]  

  • 4. [Monilethrix associated with mental debility: study of a family].
    Sfaello Z; Hariga J
    Arch Belg Dermatol Syphiligr; 1967; 23(4):363-71. PubMed ID: 5623247
    [No Abstract]   [Full Text] [Related]  

  • 5. Atrichia with cysts and mental retardation.
    Del Castillo V; Ruiz-Maldonado R; Carnevale A
    Mod Probl Paediatr; 1975; 17():21-4. PubMed ID: 1186676
    [No Abstract]   [Full Text] [Related]  

  • 6. Familial syndrome of endocrine and neuroectodermal abnormalities.
    Oerter KE; Friedman TC; Anderson HC; Cassorla FG
    Am J Med Genet; 1992 Nov; 44(4):487-91. PubMed ID: 1442893
    [TBL] [Abstract][Full Text] [Related]  

  • 7. COH1 analysis and linkage study in two Japanese families with Cohen syndrome.
    Kondo I; Shimizu A; Asakawa S; Miyamoto K; Yamagata H; Tabara Y; Shimizu N
    Clin Genet; 2005 Mar; 67(3):270-2. PubMed ID: 15691367
    [No Abstract]   [Full Text] [Related]  

  • 8. Woodhouse-Sakati syndrome: case report and symptoms review.
    Medica I; Sepcić J; Peterlin B
    Genet Couns; 2007; 18(2):227-31. PubMed ID: 17710875
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3.
    Kleefstra T; Yntema HG; Oudakker AR; de Vries BB; van Bokhoven H; Hamel BC; Poppelaars FA; Ausems MG
    Am J Med Genet; 2002 Jul; 110(4):410-1. PubMed ID: 12116222
    [No Abstract]   [Full Text] [Related]  

  • 10. Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome due to mutation of the gene MBTPS2 in a large Australian kindred.
    Ming A; Happle R; Grzeschik KH; Fischer G
    Pediatr Dermatol; 2009; 26(4):427-31. PubMed ID: 19689518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Lujan-Fryns syndrome].
    Izumikawa Y
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):117. PubMed ID: 11528648
    [No Abstract]   [Full Text] [Related]  

  • 12. A newly recognized partial alopecia syndrome associated with distinct personality traits.
    Straussberg R; Regenbogen L; Goodman RM
    J Craniofac Genet Dev Biol; 1991; 11(1):3-6. PubMed ID: 2061403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome].
    Kurosawa K
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):824-5. PubMed ID: 11529043
    [No Abstract]   [Full Text] [Related]  

  • 14. [X-linked mental retardation].
    Kurosawa K
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):826-9. PubMed ID: 11529044
    [No Abstract]   [Full Text] [Related]  

  • 15. A novel mutation in MBTPS2 causes ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome in a Chinese family.
    Ding YG; Wang JY; Qiao JJ; Mao XH; Cai SQ
    Br J Dermatol; 2010 Oct; 163(4):886-9. PubMed ID: 20854407
    [No Abstract]   [Full Text] [Related]  

  • 16. Mental retardation in the Bannayan syndrome.
    Saul RA; Stevenson RE; Bley R
    Pediatrics; 1982 May; 69(5):642-4. PubMed ID: 7079023
    [No Abstract]   [Full Text] [Related]  

  • 17. A new alopecia/mental retardation syndrome.
    Baraitser M; Carter CO; Brett EM
    J Med Genet; 1983 Feb; 20(1):64-5. PubMed ID: 6842537
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Behavioural phenotype in Börjeson-Forssman-Lehmann syndrome.
    de Winter CF; van Dijk F; Stolker JJ; Hennekam RC
    J Intellect Disabil Res; 2009 Apr; 53(4):319-28. PubMed ID: 19187102
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alopecia, macular degeneration, and growth retardation: a new syndrome?
    Küster W; Majewski F; Hammerstein W
    Am J Med Genet; 1987 Oct; 28(2):477-81. PubMed ID: 3425621
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
    J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.