Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8166

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication ; volume:1 ; number:1 ; day:28 ; month:4 ; year:2008 ; pages:1-7 ; date:12.2008
Molecular cytogenetics ; 1, Heft 1 (28.4.2008), 1-7, 12.2008

Creator: Ballif, Blake C.
Theisen, Aaron
Coppinger, Justine
Gowans, Gordon C.
Hersh, Joseph H.
Madan-Khetarpal, Suneeta
Schmidt, Karen R.
Tervo, Raymond
Escobar, Luis F.
Friedrich, Christopher A.
McDonald, Marie
Campbell, Lindsey
Ming, Jeffrey E.
Zackai, Elaine H.
Bejjani, Bassem A.
Shaffer, Lisa G.

Contributor: SpringerLink (Online service)

DOI: 10.1186/1755-8166-1-8

URN: urn:nbn:de:101:1-2019080721325506565202

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

Last update: 15.08.2025, 7:27 AM CEST

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Associated

Ballif, Blake C.
Theisen, Aaron
Coppinger, Justine
Gowans, Gordon C.
Hersh, Joseph H.
Madan-Khetarpal, Suneeta
Schmidt, Karen R.
Tervo, Raymond
Escobar, Luis F.
Friedrich, Christopher A.
McDonald, Marie
Campbell, Lindsey
Ming, Jeffrey E.
Zackai, Elaine H.
Bejjani, Bassem A.
Shaffer, Lisa G.
SpringerLink (Online service)

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Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

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Other Objects (12)

Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series

Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

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