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 *

125 related articles for article (PubMed ID: 7381873)

  • 1. Hypomelanosis of Ito with triphalangeal thumbs.
    Kukolich MK; Althaus BW; Freeman MV; Lewandowski RC
    J Med Genet; 1980 Apr; 17(2):151-2. PubMed ID: 7381873
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypomelanosis of Ito in three cases with autism and autistic-like conditions.
    Akefeldt A; Gillberg C
    Dev Med Child Neurol; 1991 Aug; 33(8):737-43. PubMed ID: 1717328
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ito syndrome (hypomelanosis of Ito) as a cause of intractable epilepsy.
    Hara M; Mitsuishi Y; Yajima K; Kozasa M; Saito K; Fukuyama Y
    Jpn J Psychiatry Neurol; 1989 Sep; 43(3):487-9. PubMed ID: 2516560
    [No Abstract]   [Full Text] [Related]  

  • 4. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.
    Bocian E; Mazurczak T; Buława E; Stańczak H; Rowicka G
    J Med Genet; 1993 Jul; 30(7):614-5. PubMed ID: 8411041
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Triphalangeal thumb in Ito's hypomelanosis syndrome.
    Vral J; De Smet L; Fabry G
    Genet Couns; 1991; 2(4):217-9. PubMed ID: 1799419
    [No Abstract]   [Full Text] [Related]  

  • 6. Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.
    Funderburk SJ; Crandall BF
    Am J Hum Genet; 1974 Nov; 26(6):715-22. PubMed ID: 4140688
    [No Abstract]   [Full Text] [Related]  

  • 7. Choanal atresia and bifid thumb associated with an abnormal D group chromosome.
    Carter CH; Smith GF; Schindeler J
    J Ment Defic Res; 1970 Sep; 14(3):221-6. PubMed ID: 5518407
    [No Abstract]   [Full Text] [Related]  

  • 8. Chromosome mosaicism in hypomelanosis of Ito.
    Ritter CL; Steele MW; Wenger SL; Cohen BA
    Am J Med Genet; 1990 Jan; 35(1):14-7. PubMed ID: 2301465
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ectodermal dysplasia and abnormal thumbs.
    Lucky AW; Esterly NB; Tunnessen WW
    J Am Acad Dermatol; 1980 May; 2(5):379-84. PubMed ID: 7381065
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypomelanosis of Ito.
    Kumar A; Chaudhary D; Bhargava V
    Indian J Pediatr; 1996; 63(4):573-5. PubMed ID: 10832484
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Menkes kinky hair syndrome in a black infant.
    Volpintesta EJ
    Am J Dis Child; 1974 Aug; 128(2):244-6. PubMed ID: 4853160
    [No Abstract]   [Full Text] [Related]  

  • 12. Tetraploidy and 18-trisomy in a six-year-old triple mosaic boy.
    Atnip RL; Summitt RL
    Cytogenetics; 1971; 10(5):305-17. PubMed ID: 5156365
    [No Abstract]   [Full Text] [Related]  

  • 13. Triphalangeal thumbs and congenital erythroid hypoplasia: report of a case with unusual features.
    Murphy S; Lubin B
    J Pediatr; 1972 Nov; 81(5):987-9. PubMed ID: 5086730
    [No Abstract]   [Full Text] [Related]  

  • 14. Hypomelanosis of Ito. Report of a case and review of the literature.
    Buzas JW; Sina B; Burnett JW
    J Am Acad Dermatol; 1981 Feb; 4(2):195-204. PubMed ID: 7217390
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.
    Koiffmann CP; de Souza DH; Diament A; Ventura HB; Alves RS; Kihara S; Wajntal A
    Am J Med Genet; 1993 Jun; 46(5):529-33. PubMed ID: 8322815
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functional Xp disomy and de novo t(X;13)(q10;q10) in a girl with hypomelanosis of Ito.
    Correa-Cerro LS; Rivera H; Vasquez AI
    J Med Genet; 1997 Feb; 34(2):161-3. PubMed ID: 9039996
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mental retardation with facial abnormalities, broad thumbs and toes and unusual dermatoglyphics.
    Davison BC; Ellis HL; Kuzemko JA; Roberts DF
    Dev Med Child Neurol; 1967 Oct; 9(5):588-93. PubMed ID: 5587707
    [No Abstract]   [Full Text] [Related]  

  • 18. [Hypomelanosis Ito in translocation trisomy 9/mosaicism (46,XX/46,XX,t(9;9)(p24;p24)). Spontaneous remission in childhood].
    Dereser-Dennl M; Brude E; König R
    Hautarzt; 2000 Sep; 51(9):688-92. PubMed ID: 11057398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletion (2)(p13p15).
    Duca D; Ioan D; Meilă P; Ionescu-Cerna M; Simionescu L; Maximilian C
    Hum Genet; 1981; 57(2):214-6. PubMed ID: 7228037
    [No Abstract]   [Full Text] [Related]  

  • 20. Hypomelanosis of Ito--a nonspecific marker of somatic mosaicism: report of case with trisomy 18 mosaicism.
    Chitayat D; Friedman JM; Johnston MM
    Am J Med Genet; 1990 Mar; 35(3):422-4. PubMed ID: 2309792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.