122 related articles for article (PubMed ID: 31187941)
1. 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]
2. 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]
3. [The Cri du Chat syndrome: a study on the quality of care].
Cerruti Mainardi P; Spunton M; Arcuri V; Pastore G; Pedrinazzi M; Nardi S; Castronovo C; Alessi D; Guala A
Minerva Pediatr; 2012 Aug; 64(4):395-400. PubMed ID: 22728611
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Cri du chat syndrome patients have DNA methylation changes in genes linked to symptoms of the disease.
Holland P; Wildhagen M; Istre M; Reiakvam OM; Dahl JA; Søraas A
Clin Epigenetics; 2022 Oct; 14(1):128. PubMed ID: 36242045
[TBL] [Abstract][Full Text] [Related]
10. Peters anomaly in cri-du-chat syndrome.
Hope WC; Cordovez JA; Capasso JE; Hammersmith KM; Eagle RC; Lall-Trail J; Levin AV
J AAPOS; 2015 Jun; 19(3):277-9. PubMed ID: 26059676
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome.
Marinescu RC; Johnson EI; Dykens EM; Hodapp RM; Overhauser J
Am J Med Genet; 1999 Sep; 86(1):66-70. PubMed ID: 10440832
[TBL] [Abstract][Full Text] [Related]
13. Parental origin of chromosome 5 deletions in the cri-du-chat syndrome.
Overhauser J; McMahon J; Oberlender S; Carlin ME; Niebuhr E; Wasmuth JJ; Lee-Chen J
Am J Med Genet; 1990 Sep; 37(1):83-6. PubMed ID: 1978567
[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. 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]
16. [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]
17. Psychomotor development in Cri du Chat Syndrome.
Cerruti Mainardi P; Guala A; Pastore G; Pozzo G; Dagna Bricarelli F; Pierluigi M
Clin Genet; 2000 Jun; 57(6):459-61. PubMed ID: 10905669
[No Abstract] [Full Text] [Related]
18. Development of diagnostic tools for the analysis of 5p deletions using interphase FISH.
Gersh M; Grady D; Rojas K; Lovett M; Moyzis R; Overhauser J
Cytogenet Cell Genet; 1997; 77(3-4):246-51. PubMed ID: 9284926
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]