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Terminal Deletion of Chromosome 10q and Its Clinical Features
Author(s) -
Kagasaka Ryoichi,
Morohoshi Teruaki,
Sawada Yohko,
Fujiwara Masaki
Publication year - 1990
Publication title -
pediatrics international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.49
H-Index - 63
eISSN - 1442-200X
pISSN - 1328-8067
DOI - 10.1111/j.1442-200x.1990.tb00788.x
Subject(s) - medicine , terminal (telecommunication) , chromosome , genetics , computational biology , gene , computer network , biology , computer science
A male case with terminal deletion of chromosome 1Oq has growth retardation, craniofacial dysmorphism, congenital heart disease and other minor anomalies. The karyotypic formula is 46, XY, del (lo), (q26.1→q ter) by a high resolution G‐banding staining. There are few differences in clinical features between our case and the previously reported cases.