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 *

175 related articles for article (PubMed ID: 32655341)

  • 1. Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal Parents.
    Alkaya DU; Karaman B; Tüysüz B
    Mol Syndromol; 2020 Jun; 11(2):97-103. PubMed ID: 32655341
    [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. 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]  

  • 4. [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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p.
    Sharma P; Gupta N; Chowdhury MR; Sapra S; Shukla R; Lall M; Kabra M
    J Pediatr Genet; 2013 Sep; 2(3):163-9. PubMed ID: 27625854
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier.
    Chernos JE; Fowlow SB; Cox DM
    Clin Genet; 1992 May; 41(5):266-9. PubMed ID: 1606717
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Cri-du-Chat Syndrome Cytogenetically Cryptic Recombination Aneusomy of Chromosome 5: Implications in Recurrence Risk Estimation.
    Ohnuki Y; Torii C; Kosaki R; Yagihashi T; Sago H; Hayashi K; Yasukawa K; Takahashi T; Kosaki K
    Mol Syndromol; 2010; 1(2):95-98. PubMed ID: 21045963
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microarray delineation of familial chromosomal imbalance with deletion 5q35 and duplication 10q25 in a child showing multiple anomalies and dysmorphism.
    Masri A; Gimelli S; Hamamy H; Sloan-Béna F
    Am J Med Genet A; 2014 May; 164A(5):1254-61. PubMed ID: 24478242
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia.
    Tsao CY; Wenger GD; Bartholomew DW
    Am J Med Genet A; 2005 Apr; 134A(2):198-201. PubMed ID: 15690344
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. 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]  

  • 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. 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]  

  • 18. 5p;12q translocation with manifestations of cri du chat syndrome and Marfanoid arachnodactyly.
    Zhang SZ; Tang YC; Dai FP; Niebuhr E
    Clin Genet; 1990 Feb; 37(2):153-7. PubMed ID: 2311266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome.
    Marinescu RC; Johnson EI; Grady D; Chen XN; Overhauser J
    Clin Genet; 1999 Oct; 56(4):282-8. PubMed ID: 10636446
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal detection of cri du chat syndrome on uncultured amniocytes using fluorescence in situ hybridization (FISH).
    Pettenati MJ; Hayworth R; Cox K; Rao PN
    Clin Genet; 1994 Jan; 45(1):17-20. PubMed ID: 8149646
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.