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4
results
ghr-summaries.xml
... arm of the chromosome in a region designated
q22
.3. This chromosomal change is associated with delayed ... db-key ><db >ICD-10-CM</db><key >
Q22
.0</key></db-key><db-key ><db >ICD- ...
Most Recent PubMed Articles
17q21
.32-
q22
Deletion in a girl with osteogenesis imperfecta, tricho-dento-osseous syndrome, and
intellectual disability
.
Localization of a second NM23
gene
, NME2, to
chromosome
17q21-q22
.
Localization of the
gene
(SYM1) for proximal symphalangism to
human
chromosome
17q21-q22
.
More articles »