"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8166

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: "Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes ; volume:5 ; number:1 ; day:29 ; month:1 ; year:2012 ; pages:1-5 ; date:12.2012
Molecular cytogenetics ; 5, Heft 1 (29.1.2012), 1-5, 12.2012

Creator: Rafati, Maryam
Seyyedaboutorabi, Elaheh
Ghadirzadeh, Mohammad R.
Heshmati, Yaser
Adibi, Homeira
Keihanidoust, Zarrintaj
Eshraghian, Mohammad R.
Javadi, Gholam Reza
Dastan, Jila
Mosavi-Jarrahi, Alireza
Hoseini, Azadeh
Purhoseini, Marzieh
Ghaffari, Saeed R.

Contributor: SpringerLink (Online service)

DOI: 10.1186/1755-8166-5-9

URN: urn:nbn:de:101:1-2021081721053438754540

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:54 AM CEST

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Associated

Rafati, Maryam
Seyyedaboutorabi, Elaheh
Ghadirzadeh, Mohammad R.
Heshmati, Yaser
Adibi, Homeira
Keihanidoust, Zarrintaj
Eshraghian, Mohammad R.
Javadi, Gholam Reza
Dastan, Jila
Mosavi-Jarrahi, Alireza
Hoseini, Azadeh
Purhoseini, Marzieh
Ghaffari, Saeed R.
SpringerLink (Online service)

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"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes

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Other Objects (12)

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability

A comprehensive list of human microdeletion and microduplication syndromes

Differences Between Familial and Sporadic Celiac Disease

Familial inheritance of the 3q29 microdeletion syndrome: case report and review

Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report

Familial microdeletion 18p11.32 to 18p11.31 in a Chinese family with normal phenotype

The use of fluorescence in situhybridization techniques in the detection of microdeletion syndromes

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Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas

Imaging Familial and Sporadic Neurodegenerative Disorders Associated with Parkinsonism

Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations

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A comprehensive list of human microdeletion and microduplication syndromes

Differences Between Familial and Sporadic Celiac Disease

Familial inheritance of the 3q29 microdeletion syndrome: case report and review

Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report

Familial microdeletion 18p11.32 to 18p11.31 in a Chinese family with normal phenotype

The use of fluorescence in situhybridization techniques in the detection of microdeletion syndromes

Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA

Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas

Imaging Familial and Sporadic Neurodegenerative Disorders Associated with Parkinsonism

Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

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A comprehensive list of human microdeletion and microduplication syndromes

Differences Between Familial and Sporadic Celiac Disease

Familial inheritance of the 3q29 microdeletion syndrome: case report and review

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