Greig Cephalopolysyndactyly (GCPS) Contiguous Gene Syndrome in a Boy with a 14 Mb Deletion in Region 7p13-14 Caused by a Paternal Balanced Insertion (5; 7) [Expression of Concern]
Schulz S, Volleth M, Muschke P, Wieland I, Wieacker P. Appl Clin Genet. 2008;1:19–22.The Editor-in-Chief and Publisher of The Application of Clinical Genetics wish to issue an Expression of Concern for the above published article.The original article contained a...
Main Authors: | Schulz S, Volleth M, Muschke P, Wieland I, Wieacker P |
---|---|
Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2021-03-01
|
Series: | The Application of Clinical Genetics |
Subjects: | |
Online Access: | https://www.dovepress.com/expression-of-concern-greig-cephalopolysyndactyly-gcps-contiguous-gene-peer-reviewed-article-TACG |
Similar Items
-
Greig cephalopolysyndactyly (GCPS) contiguous gene syndrome in a boy with a 14 Mb deletion in region 7p13-14 caused by a paternal balanced insertion (5; 7)
by: Solveig Schulz, et al.
Published: (2008-11-01) -
Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
by: Kinga Kozma, et al.
Published: (2021-10-01) -
Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreas
by: Saki Ito, et al.
Published: (2018-01-01) -
Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report
by: Martina Siracusano, et al.
Published: (2019-04-01) -
Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family
by: Evelina Siavrienė, et al.
Published: (2019-09-01)