BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 23926013)

  • 1. [Analysis of copy number variations in an infant with Cri du Chat syndrome by array-based comparative genomic hybridization].
    Luo FW; Luo CQ; Xie JS; Gen Q; Liu H; Li F; Chen WB; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):443-6. PubMed ID: 23926013
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. A de novo chromosomal abnormality in Cri du Chat syndrome.
    Sun SC; Luo FW; Zhou ZM; Peng YS; Song HW
    Indian J Pediatr; 2014 Jul; 81(7):722-5. PubMed ID: 23900752
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [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]  

  • 10. Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri-du-chat syndrome in addition to a partial duplication of CTNND2.
    Sardina JM; Walters AR; Singh KE; Owen RX; Kimonis VE
    Am J Med Genet A; 2014 Jul; 164A(7):1761-4. PubMed ID: 24677774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Accidental finding of a cri du chat syndrome in an adult patient by means of array-CGH].
    Ferreirós-Martínez R; López-Manzanares L; Alonso-Cerezo C
    Rev Neurol; 2014 Jul; 59(2):71-6. PubMed ID: 25005318
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
    Chen CP; Wang LK; Chern SR; Wu PS; Ko K; Chen YN; Chen SW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):591-5. PubMed ID: 27590389
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
    Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG
    Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization.
    Zhang X; Snijders A; Segraves R; Zhang X; Niebuhr A; Albertson D; Yang H; Gray J; Niebuhr E; Bolund L; Pinkel D
    Am J Hum Genet; 2005 Feb; 76(2):312-26. PubMed ID: 15635506
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of array comparative genomic hybridization in prenatal diagnosis of a case with 5q35 deletion syndrome].
    Feng Z; Hu H; Mao C; Wang D; Liu L; Liu S; Jing Z; Liu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):240-243. PubMed ID: 28397228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Molecular approach to analyzing the human 5p deletion syndrome, cri du chat.
    Carlock LR; Wasmuth JJ
    Somat Cell Mol Genet; 1985 May; 11(3):267-76. PubMed ID: 2988137
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.