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 *

120 related articles for article (PubMed ID: 3573005)

  • 21. Subtelomeric fish findings in Turkish patients with idiopathic mental retardation.
    Tos T; Vurucu S; Karkucak M; Kozan S; Gul D; Akin R
    Genet Couns; 2013; 24(3):259-64. PubMed ID: 24341139
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.
    Nielsen KB; Egede F; Mouridsen I; Mohr J
    J Med Genet; 1979 Dec; 16(6):461-6. PubMed ID: 537020
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.
    Moncla A; Livet MO; Auger M; Mattei JF; Mattei MG; Giraud F
    J Med Genet; 1991 Sep; 28(9):627-32. PubMed ID: 1956064
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Deleted ring chromosome 22 in a mentally retarded boy.
    Gustavson KH; Arancibia W; Eriksson U; Svennerholm L
    Clin Genet; 1986 Apr; 29(4):337-41. PubMed ID: 2872982
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.
    Watt JL; Olson IA; Johnston AW; Ross HS; Couzin DA; Stephen GS
    J Med Genet; 1985 Aug; 22(4):283-7. PubMed ID: 4045954
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Cytogenetic and molecular characterization of a patient with partial 6q trisomy and 1q monosomy].
    Qin F; Lu X; Feng Y; Tang P; Niu G; Li F; Zhang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):231-4. PubMed ID: 27060323
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
    Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial monosomy 7q.
    Ponnala R; Dalal A
    Indian Pediatr; 2011 May; 48(5):399-401. PubMed ID: 21654006
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The neuropsychiatry and multisystem features of the Smith-Magenis syndrome: a review.
    Shelley BP; Robertson MM
    J Neuropsychiatry Clin Neurosci; 2005; 17(1):91-7. PubMed ID: 15746488
    [TBL] [Abstract][Full Text] [Related]  

  • 30. De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature.
    Weise A; Rittinger O; Starke H; Ziegler M; Claussen U; Liehr T
    Cytogenet Genome Res; 2003; 103(1-2):14-6. PubMed ID: 15004457
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Terminal deletion of the long arm of chromosome 10.
    Scigliano S; Grégoire MJ; Schmitt M; Jonveaux PH; LeHeup B
    Clin Genet; 2004 Apr; 65(4):294-8. PubMed ID: 15025722
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation.
    Dirse V; Burnyte B; Gineikiene E; Griskevicius L; Utkus A
    J Genet; 2014 Aug; 93(2):501-3. PubMed ID: 25189247
    [No Abstract]   [Full Text] [Related]  

  • 33. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).
    Brusnický J; van Heerden KM; de Jong G; Cronjé AS; Retief AE
    J Med Genet; 1986 Oct; 23(5):435-45. PubMed ID: 3783620
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Terminal deletion (14)(q32.3): a new case.
    Telford N; Thomson DA; Griffiths MJ; Ilett S; Watt JL
    J Med Genet; 1990 Apr; 27(4):261-3. PubMed ID: 2182875
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 cases.
    Poot M; Verrijn Stuart AA; van Daalen E; van Iperen A; van Binsbergen E; Hochstenbach R
    Eur J Med Genet; 2013 Jul; 56(7):346-50. PubMed ID: 23603061
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Chromosome 10qter deletion syndrome: a review and report of three new cases.
    Wulfsberg EA; Weaver RP; Cunniff CM; Jones MC; Jones KL
    Am J Med Genet; 1989 Mar; 32(3):364-7. PubMed ID: 2658586
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Partial trisomy 10p in combination with partial monosomy 20p--a syndrome with muscular hypotonia, psychomotor retardation, dwarfism and craniofacial dysmorphia].
    Meyer R
    Klin Padiatr; 1990; 202(5):352-4. PubMed ID: 2214595
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability.
    Chen CP; Lin SP; Chern SR; Tsai FJ; Lee MS; Chen YJ; Wang W
    Genet Couns; 2011; 22(4):425-30. PubMed ID: 22303804
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Familial presentation of microdeletion and inverted microduplication with array-CGH].
    Beseler-Soto B; Jiménez-Candel MI; Pedrón-Marzal G; Pérez-García B; Carpena-Lucas PJ
    Rev Neurol; 2014 Dec; 59(12):551-4. PubMed ID: 25501453
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Chromosome 13 deletion syndrome: report of a new case and discussion of the different etiologic patterns of retinoblastoma.
    Lungarotti MS; Mariotti G; Quarta C; Delogu A; Fiore C
    Ophthalmologica; 1980; 181(5):245-50. PubMed ID: 7243183
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.