Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanningRUNX2 andVEGF

Authors :: Naohisa Yahagi
Rika Kosaki
Kenjiro Kosaki
Takao Takahashi
Yoko Naito
Gen Nishimura
Noboru Hosokai
Yasushi Fujii
Kosuke Izumi
Masataka Higuchi
Source :: American Journal of Medical Genetics Part A. :398-401
Publication Year :: 2006
Publisher :: Wiley, 2006.

Subjects :: Pathology
medicine.medical_specialty
Cleidocranial Dysplasia
biology
business.industry
VEGF receptors
Gene deletion
medicine.disease
Osteochondrodysplasia
RUNX2
Endocrinology
Gene mapping
Internal medicine
Genetics
medicine
biology.protein
business
Genetics (clinical)

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