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Changing facial phenotype in Cohen syndrome: towards clues for an ...
www.nature.com
Clinical and molecular characterization of Italian patients ...
www.nature.com
Changing facial phenotype in Cohen syndrome: towards clues for an ...
www.nature.com
A, B) Two patients, aged 4 and 19 years, with Cohen syndrome ...
www.researchgate.net
Changing facial phenotype in Cohen syndrome: towards clues for an ...
www.nature.com
Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1 ...
www.cell.com
Cohen syndrome: MedlinePlus Genetics
medlineplus.gov
Changing facial phenotype in Cohen syndrome: towards clues for an ...
www.nature.com
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www.semanticscholar.org
Allelic Heterogeneity in the COH1 Gene Explains Clinical ...
www.cell.com
Changing facial phenotype in Cohen syndrome: towards clues for an ...
www.nature.com
Cohen Syndrome | SpringerLink
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www.cell.com
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www.semanticscholar.org
Cohen syndrome: MedlinePlus Genetics
medlineplus.gov
High frequency of COH1 intragenic deletions and duplications ...
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Cohen Syndrome | SpringerLink
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Changing facial phenotype in Cohen syndrome: towards clues for an ...
www.nature.com
Typical facial features of patients with CS. Shown are patients 8 ...
www.researchgate.net
First case report of Cohen syndrome in the Tunisian population ...
bmcmedgenet.biomedcentral.com
Early Diagnostic Signs and the Natural History of Typical Findings ...
www.sciencedirect.com
Research Cohen Syndrome
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Cohen syndrome: MedlinePlus Genetics
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Figure 2 from Cohen syndrome with neutropenia-induced ...
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Frontiers | A Novel Homozygous VPS13B Splice-Site Mutation Causing ...
www.frontiersin.org
MENA Congress for Rare Diseases | June 21 is Cohen Syndrome ...
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Cohen syndrome: Report of nine cases and review of the literature ...
www.sciencedirect.com
Cohen syndrome - Wikipedia
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Figure 1 from Cohen syndrome with neutropenia-induced ...
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A novel VPS13B mutation in Cohen syndrome: a case report and ...
bmcmedgenet.biomedcentral.com
Genetic Clinics
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Allelic Heterogeneity in the COH1 Gene Explains Clinical ...
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Research Cohen Syndrome
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Cystoid Macular Edema in a 10-Year-Old Boy With Cohen Syndrome
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Identification of a Mutation in VPS13B , the Cohen Syndrome Gene ...
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Cells | Free Full-Text | Ultrastructural Abnormalities in Induced ...
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of clinical signs with percentages between Cohen syndrome patients ...
www.researchgate.net
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Cohen Syndrome - Cohen Syndrome on Vimeo
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Individual 12-Cohen syndrome, MIM 216550. (A) Dysmorphic features ...
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Arquivos Brasileiros de Oftalmologia - Ocular findings in ...
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Functional Analysis of a Compound Heterozygous Mutation in the ...
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Major and minor criteria for diagnosis of Cohen syndrome The ...
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EED and EZH2 constitutive variants: A study to expand the Cohen ...
onlinelibrary.wiley.com
Figure 3 from Cohen syndrome with neutropenia-induced ...
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Cohen syndrome: MedlinePlus Genetics
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