BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

473 related articles for article (PubMed ID: 10434125)

  • 1. Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studies.
    Reddy KS; Smith DL; Ball CS
    Ann Genet; 1999; 42(2):105-8. PubMed ID: 10434125
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
    Sreekantaiah C; Kronn D; Marinescu RC; Goldin B; Overhauser J
    Am J Med Genet; 1999 Sep; 86(3):264-8. PubMed ID: 10482877
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
    Laczmanska I; Stembalska A; Gil J; Czemarmazowicz H; Sasiadek M
    Eur J Med Genet; 2006; 49(1):87-92. PubMed ID: 16473315
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome.
    Elmakky A; Carli D; Lugli L; Torelli P; Guidi B; Falcinelli C; Fini S; Ferrari F; Percesepe A
    Eur J Med Genet; 2014 Mar; 57(4):145-50. PubMed ID: 24556499
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetic analysis of a case with atypical neonatal Cri-du-chat syndrome].
    He W; Chen H; Mu H; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):104-106. PubMed ID: 29419873
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization.
    Bernstein R; Bocian ME; Cain MJ; Bengtsson U; Wasmuth JJ
    Am J Med Genet; 1993 Apr; 46(1):77-82. PubMed ID: 8494035
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
    Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic evaluation, fluorescence in situ hybridization, and molecular study of psu idic(X)(pter-->q22.3::q22.3-->pter) chromosome abberation in a girl with moderate growth retardation.
    Petković I; Barisić I; Bago R
    Croat Med J; 2003 Aug; 44(4):494-9. PubMed ID: 12950157
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis.
    Cornish KM; Cross G; Green A; Willatt L; Bradshaw JM
    J Med Genet; 1999 Jul; 36(7):567-70. PubMed ID: 10424821
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).
    Scheuerle A; Zenger-Hain JL; Van Dyke DL; Ledbetter DH; Greenberg F; Shaffer LG
    Am J Med Genet; 1995 May; 56(4):403-8. PubMed ID: 7604850
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
    Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D; Boccone L; Ristaldi MS; Nucaro AL
    Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic and phoniatric findings in mosaic cri du chat syndrome.
    Romano C; Ragusa RM; Scillato F; Greco D; Amato G; Barletta C
    Am J Med Genet; 1991 Jun; 39(4):391-5. PubMed ID: 1877615
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat).
    Levy B; Dunn TM; Kern JH; Hirschhorn K; Kardon NB
    Am J Med Genet; 2002 Mar; 108(3):192-7. PubMed ID: 11891684
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    Canún S; Mutchinick O; Shaffer LG; Fernández C
    Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome.
    Goodart SA; Simmons AD; Grady D; Rojas K; Moyzis RK; Lovett M; Overhauser J
    Genomics; 1994 Nov; 24(1):63-8. PubMed ID: 7896290
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A phenotypically normal female with pseudodicentric X: correlation for statural genes.
    Gole LA; Annapoorna V; Lim J; Anandakumar C
    Singapore Med J; 2001 Sep; 42(9):428-9. PubMed ID: 11811611
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
    Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.