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 *

135 related articles for article (PubMed ID: 3023617)

  • 1. Intrachromosomal insertion of chromosome 13 in a family with psychosis and mental subnormality.
    Roberts SH; Cowie VA; Singh KR
    J Ment Defic Res; 1986 Sep; 30 ( Pt 3)():227-32. PubMed ID: 3023617
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome studies on male patients at a mental subnormality hospital.
    Aitken J; Brunton M; Jacobs PA; Price WH; MacColl K
    Clin Genet; 1971; 2(6):338-46. PubMed ID: 5155310
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ; Planteydt HT; Hagemeijer A; Peters-Slough MF; Timmerman MJ
    Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial pericentric inversion inv(8)(p23q11).
    Boyd H; Kaste J; Hovi E; Ritanen-Mohammed UM; Kääriäinen H; de la Chapelle A; Lehesjoki AE
    J Med Genet; 1994 Mar; 31(3):201-5. PubMed ID: 8014967
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.
    Barber JC; Ellis KH; Bowles LV; Delhanty JD; Ede RF; Male BM; Eccles DM
    J Med Genet; 1994 Apr; 31(4):312-6. PubMed ID: 8071957
    [TBL] [Abstract][Full Text] [Related]  

  • 6. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.
    Smeets D; van Ravenswaaij C; de Pater J; Gerssen-Schoorl K; Van Hemel J; Janssen G; Smits A
    J Med Genet; 1997 Jan; 34(1):18-23. PubMed ID: 9032644
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion.
    Lybaek H; Ørstavik KH; Prescott T; Hovland R; Breilid H; Stansberg C; Steen VM; Houge G
    Eur J Hum Genet; 2009 Jul; 17(7):904-10. PubMed ID: 19156171
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomes and mental retardation.
    Baraitser M
    Psychol Med; 1986 Aug; 16(3):495-7. PubMed ID: 2945219
    [No Abstract]   [Full Text] [Related]  

  • 9. Duplication of the long arm of chromosome 13 secondary to a recombination in a maternal intrachromosomal insertion (shift).
    Vekemans M; Morichon-Delvallez N
    Prenat Diagn; 1990 Dec; 10(12):787-94. PubMed ID: 1963687
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter).
    Goldstein DJ; Ward RE; Nichols WC; Palmer CG
    J Med Genet; 1987 Nov; 24(11):684-7. PubMed ID: 3430543
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic causes of mental subnormality.
    Lancet; 1973 Jul; 2(7820):83-4. PubMed ID: 4123630
    [No Abstract]   [Full Text] [Related]  

  • 12. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 13. Partial trisomy 4p resulting from a balanced intrachromosomal insertion, 4(q313p14p16).
    Hastings R; Hamer B; Roth S; Lucas M
    Clin Genet; 1990 Aug; 38(2):121-5. PubMed ID: 2170065
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial 13p+ chromosome with mental retardation and dysmorphic features of two children.
    Stoll C; Rohmer A; Korn R; Heumann G
    Hum Genet; 1976 Sep; 34(1):81-4. PubMed ID: 965011
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects.
    Shim SH; Wyandt HE; McDonald-McGinn DM; Zackai EZ; Milunsky A
    Clin Genet; 2004 Jul; 66(1):46-52. PubMed ID: 15200507
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Present possibilities for the prevention of hereditary mental subnormality.
    Czeizel A; Métneki-Bajomi J
    Int J Rehabil Res; 1978 Jul; 1(3):301-8. PubMed ID: 748188
    [No Abstract]   [Full Text] [Related]  

  • 17. Psychotic manifestations in a patient with mental retardation and a 6.2 megabase deletion at the distal short arm of chromosome 12.
    Velinov M; Beldia G; Gu H; Tsiouris JA; Jenkins EC; Brown WT
    CNS Spectr; 2008 Jun; 13(6):515-9. PubMed ID: 18567976
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversion.
    Ramer JC; Mowrey PN; Ladda RL
    Clin Genet; 1991 Jun; 39(6):442-50. PubMed ID: 1863992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a mentally retarded boy with a piebald trait, due to maternal insertion, ins(8;4).
    Fujimoto A; Reddy KS; Spinks R
    Am J Med Genet; 1998 Jan; 75(1):78-81. PubMed ID: 9450862
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities].
    Gregori Romero M; Gil Benso R; López Ginés C; Pellín Pérez A; Barberá Guillem E
    An Esp Pediatr; 1984 Oct; 21(6):593-6. PubMed ID: 6524770
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.