BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 25820652)

  • 1. Anesthesia in Cri du Chat syndrome: Information on 51 Italian patients.
    Guala A; Spunton M; Mainardi PC; Emmig U; Acucella G; Danesino C
    Am J Med Genet A; 2015 May; 167A(5):1168-70. PubMed ID: 25820652
    [No Abstract]   [Full Text] [Related]  

  • 2. Cri du Chat Syndrome: a case report from Ghana.
    Badoe EV
    West Afr J Med; 2014; 33(2):154-6. PubMed ID: 25236835
    [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. The first three mosaic cri du chat syndrome patients with two rearranged cell lines.
    Perfumo C; Cerruti Mainardi P; Calí A; Coucourde G; Zara F; Cavani S; Overhauser J; Bricarelli FD; Pierluigi M
    J Med Genet; 2000 Dec; 37(12):967-72. PubMed ID: 11186943
    [No Abstract]   [Full Text] [Related]  

  • 5. Cri du chat syndrome.
    Iyer SL; Duraiswamy A; Kher AS; Joshi S; Bharucha BA; Kanade S
    J Postgrad Med; 1996; 42(3):86-8. PubMed ID: 9715326
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Fertility and the cri du chat syndrome.
    Martínez JE; Tuck-Muller CM; Superneau D; Wertelecki W
    Clin Genet; 1993 Apr; 43(4):212-4. PubMed ID: 8330455
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?
    Choong YF; Watts P; Little E; Beck L
    J AAPOS; 2003 Jun; 7(3):226-7. PubMed ID: 12825068
    [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. del5p/dup5q in a 'cri du chat' patient without parental chromosomal rearrangement.
    Akalin I; Yararbas K; Akgul N; Babaoglu E; Akay GG; Dyer S; Kutlay NY; Ruhi HI; Kog G; Tukun A
    Am J Med Genet A; 2006 May; 140(9):1016-20. PubMed ID: 16619202
    [No Abstract]   [Full Text] [Related]  

  • 11. Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndrome.
    Goodart SA; Butler MG; Overhauser J
    Hum Genet; 1996 Jun; 97(6):802-7. PubMed ID: 8641700
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The natural history of Cri du Chat Syndrome. A report from the Italian Register.
    Mainardi PC; Pastore G; Castronovo C; Godi M; Guala A; Tamiazzo S; Provera S; Pierluigi M; Bricarelli FD
    Eur J Med Genet; 2006; 49(5):363-83. PubMed ID: 16473053
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition.
    Kjaer I; Niebuhr E
    Am J Med Genet; 1999 Jan; 82(1):6-14. PubMed ID: 9916835
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Cri-du-chat syndrome--a case report].
    Chiu CP; Lin TY
    Changgeng Yi Xue Za Zhi; 1986 Jun; 9(2):134-8. PubMed ID: 3454700
    [No Abstract]   [Full Text] [Related]  

  • 16. Skin picking disorder in 97 Italian and Spanish Cri du chat patients.
    Spunton M; Guala A; Liverani ME; Medolago L; Tognon F; Casado F; Del Valle M; Porras J; Larrea I; Porta G; Albani G; Nevado J; Danesino C
    Am J Med Genet A; 2019 Aug; 179(8):1525-1530. PubMed ID: 31187941
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new genomic mechanism leading to cri-du-chat syndrome.
    South ST; Swensen JJ; Maxwell T; Rope A; Brothman AR; Chen Z
    Am J Med Genet A; 2006 Dec; 140(24):2714-20. PubMed ID: 17103439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Two cases of cri-du-chat syndrome with mild phenotypic effect but with different size of 5p deletion.
    Smith A; Field B; Murray R; Nelson J
    J Paediatr Child Health; 1990 Jun; 26(3):152-4. PubMed ID: 2206616
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 7.