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Items: 1 to 20 of 101

1.

Anesthetic experience of a patient with cri du chat syndrome.

Han I, Kim YS, Kim SW.

Korean J Anesthesiol. 2013 Nov;65(5):482-3. doi: 10.4097/kjae.2013.65.5.482. No abstract available.

2.

Anesthetic management of a patient with Cri Du Chat syndrome. Case report.

dos Santos KM, de Rezende DC, Borges ZD.

Rev Bras Anestesiol. 2010 Nov-Dec;60(6):630-3, 350-1. doi: 10.1016/S0034-7094(10)70078-7. English, Portuguese.

3.

A systematic review of the oral and craniofacial manifestations of cri du chat syndrome.

Corcuera-Flores JR, Casttellanos-Cosano L, Torres-Lagares D, Serrera-Figallo MÁ, Rodríguez-Caballero Á, Machuca-Portillo G.

Clin Anat. 2016 Jul;29(5):555-60. doi: 10.1002/ca.22654. Epub 2015 Dec 21. Review.

PMID:
26457586
4.

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 1;24(1):63-8.

PMID:
7896290
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. doi: 10.1016/j.ejmg.2014.02.005. Epub 2014 Feb 18.

PMID:
24556499
6.

Progressive scoliosis in cri-du-chat syndrome over a 20-year follow-up period: a case report.

Saito N, Ebara S, Fukushima Y, Wakui K, Takaoka K.

Spine (Phila Pa 1976). 2001 Apr 1;26(7):835-7.

PMID:
11295909
7.

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. doi: 10.1002/ajmg.a.36494. Epub 2014 Mar 26.

PMID:
24677774
8.

Determination of periodontopathogens in patients with Cri du chat syndrome.

Ballesta-Mudarra S, Machuca-Portillo G, Torres-Lagares D, Rodríguez-Caballero Á, Yáñez-Vico RM, Solano-Reina E, Perea-Pérez E.

Med Oral Patol Oral Cir Bucal. 2013 Nov 1;18(6):e883-7.

9.

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.

PMID:
12825068
11.

Brain stem hypoplasia associated with Cri-du-Chat syndrome.

Hong JH, Lee HY, Lim MK, Kim MY, Kang YH, Lee KH, Cho SG.

Korean J Radiol. 2013 Nov-Dec;14(6):960-2. doi: 10.3348/kjr.2013.14.6.960. Epub 2013 Nov 5.

12.

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. Epub 2010 Aug 13.

13.

Assessment of orofacial characteristics and oral pathology associated with cri-du-chat syndrome.

Rodríguez-Caballero A, Torres-Lagares D, Yáñez-Vico RM, Gutiérrez-Pérez JL, Machuca-Portillo G.

Oral Dis. 2012 Mar;18(2):191-7. doi: 10.1111/j.1601-0825.2011.01864.x. Epub 2011 Oct 30.

PMID:
22035137
14.

[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. doi: 10.3760/cma.j.issn.1003-9406.2013.01.021. Chinese.

PMID:
23450488
15.

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.

PMID:
1606717
16.

Psychomotor development in 65 home-reared children with cri-du-chat syndrome.

Wilkins LE, Brown JA, Wolf B.

J Pediatr. 1980 Sep;97(3):401-5.

PMID:
7411302
17.

Unusual ocular findings in an infant with cri-du-chat syndrome.

Kitsiou-Tzeli S, Dellagrammaticas HD, Papas CB, Ladas ID, Bartsocas CS.

J Med Genet. 1983 Aug;20(4):304-7.

18.

Developmental and behavioural characteristics of cri du chat syndrome.

Cornish KM, Pigram J.

Arch Dis Child. 1996 Nov;75(5):448-50.

19.

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.

PMID:
8641700
20.

Prenatal diagnosis of cri du chat (5p-) syndrome in association with isolated moderate bilateral ventriculomegaly.

Stefanou EG, Hanna G, Foakes A, Crocker M, Fitchett M.

Prenat Diagn. 2002 Jan;22(1):64-6.

PMID:
11810654

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