Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations-Reference-Cited by-同舟云学术

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations

Published:2020-09 Issue: Volume:28 Page:110-119
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Villa R.,Fergnani V.G.C.,Silipigni R.,Guerneri S.,Cinnante C.,Guala A.,Danesino C.,Scola E.^ORCID,Conte G.^ORCID,Fumagalli M.,Gangi S.,Colombo L.,Picciolini O.,Ajmone P.F.,Accogli A.,Madia F.,Tassano E.,Scala M.,Capra V.,Srour M.,Spaccini L.,Righini A.,Greco D.,Castiglia L.,Romano C.,Bedeschi M.F.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference70 articles.

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2. Cytologic observations in 35 individuals with a 5p- karyotype;Niebuhr;Hum. Genet.,1978

3. Cri du Chat syndrome;Cerruti Mainardi;Orphanet J. Rare Dis.,2006

4. The natural history of Cri du Chat Syndrome. A report from the Italian Register;Mainardi;Eur. J. Med. Genet.,2006

5. Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation;Mainardi;J. Med. Genet.,2001

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