BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 11238681)

  • 21. Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR.
    Wu Q; Niebuhr E; Yang H; Hansen L
    Eur J Hum Genet; 2005 Apr; 13(4):475-85. PubMed ID: 15657623
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5p.
    Shapiro AJ; Weck KE; Chao KC; Rosenfeld M; Nygren AO; Knowles MR; Leigh MW; Zariwala MA
    J Pediatr; 2014 Oct; 165(4):858-61. PubMed ID: 25066065
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Regulation of the rapsyn promoter by kaiso and delta-catenin.
    Rodova M; Kelly KF; VanSaun M; Daniel JM; Werle MJ
    Mol Cell Biol; 2004 Aug; 24(16):7188-96. PubMed ID: 15282317
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The human telomere terminal transferase enzyme is a ribonucleoprotein that synthesizes TTAGGG repeats.
    Morin GB
    Cell; 1989 Nov; 59(3):521-9. PubMed ID: 2805070
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cri-du-chat.
    Sigafoos J; O'Reilly MF; Lancioni GE
    Dev Neurorehabil; 2009 Jun; 12(3):119-21. PubMed ID: 19466618
    [No Abstract]   [Full Text] [Related]  

  • 26. Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.
    Azman BZ; Akhir SM; Zilfalil BA; Ankathil R
    Singapore Med J; 2008 Apr; 49(4):e98-e100. PubMed ID: 18418516
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Delta-catenin is required for the maintenance of neural structure and function in mature cortex in vivo.
    Matter C; Pribadi M; Liu X; Trachtenberg JT
    Neuron; 2009 Nov; 64(3):320-7. PubMed ID: 19914181
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genotype-phenotype correlation of 5p-syndrome: pitfall of diagnosis.
    Kondoh T; Shimokawa O; Harada N; Doi T; Yun C; Gohda Y; Kinoshita F; Matsumoto T; Moriuchi H
    J Hum Genet; 2005; 50(1):26-29. PubMed ID: 15602631
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
    Conlin LK; Thiel BD; Bonnemann CG; Medne L; Ernst LM; Zackai EH; Deardorff MA; Krantz ID; Hakonarson H; Spinner NB
    Hum Mol Genet; 2010 Apr; 19(7):1263-75. PubMed ID: 20053666
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Breakpoint delineation in 5p- patients leads to new insights about microcephaly and the typical high-pitched cry.
    Chehimi SN; Zanardo ÉA; Ceroni JRM; Nascimento AM; Madia FAR; Dias AT; Filho GMN; Montenegro MM; Damasceno J; Costa TVMM; Gasparini Y; Kim CA; Kulikowski LD
    Mol Genet Genomic Med; 2020 Feb; 8(2):e957. PubMed ID: 31568707
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A clue in the diagnosis of Cri-du-chat syndrome: Pontine hypoplasia.
    Uzunhan TA; Sayınbatur B; Calışkan M; Sahin A; Aydın K
    Ann Indian Acad Neurol; 2014 Apr; 17(2):209-10. PubMed ID: 25024576
    [No Abstract]   [Full Text] [Related]  

  • 32. Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.
    Fang JS; Lee KF; Huang CT; Syu CL; Yang KJ; Wang LH; Liao DL; Chen CH
    Clin Genet; 2008 Jun; 73(6):585-90. PubMed ID: 18400035
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Deletion of the neuron-specific protein delta-catenin leads to severe cognitive and synaptic dysfunction.
    Israely I; Costa RM; Xie CW; Silva AJ; Kosik KS; Liu X
    Curr Biol; 2004 Sep; 14(18):1657-63. PubMed ID: 15380068
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A survey of the prevalence of stereotypy, self-injury and aggression in children and young adults with Cri du Chat syndrome.
    Collins MS; Cornish K
    J Intellect Disabil Res; 2002 Feb; 46(Pt 2):133-40. PubMed ID: 11869383
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Temperature-dependent sex determination in the snapping turtle: manipulation of the embryonic sex steroid environment.
    Rhen T; Lang JW
    Gen Comp Endocrinol; 1994 Nov; 96(2):243-54. PubMed ID: 7851724
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Terminal deletion of the short arm of chromosome 5.
    Baccichetti C; Lenzini E; Artifoni L; Caufin D; Marangoni P
    Clin Genet; 1988 Oct; 34(4):219-23. PubMed ID: 3233775
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multigenerational autosomal dominant inheritance of 5p chromosomal deletions.
    Zhang B; Willing M; Grange DK; Shinawi M; Manwaring L; Vineyard M; Kulkarni S; Cottrell CE
    Am J Med Genet A; 2016 Mar; 170(3):583-93. PubMed ID: 26601658
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
    Kaminsky EB; Kaul V; Paschall J; Church DM; Bunke B; Kunig D; Moreno-De-Luca D; Moreno-De-Luca A; Mulle JG; Warren ST; Richard G; Compton JG; Fuller AE; Gliem TJ; Huang S; Collinson MN; Beal SJ; Ackley T; Pickering DL; Golden DM; Aston E; Whitby H; Shetty S; Rossi MR; Rudd MK; South ST; Brothman AR; Sanger WG; Iyer RK; Crolla JA; Thorland EC; Aradhya S; Ledbetter DH; Martin CL
    Genet Med; 2011 Sep; 13(9):777-84. PubMed ID: 21844811
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature.
    Su J; Fu H; Xie B; Lu W; Li W; Wei Y; Zhang Q; Wei S; Chen Q; Lu Y; Jiang T; Luo J; Qin Z
    Mol Cytogenet; 2019; 12():49. PubMed ID: 31827621
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

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