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Syndrome de microduplication 16p13.11
Syndrome de microduplication 16p13.3
Syndrome de microdélétion 16p13.11

Translation of "syndrome de microdélétion 16p13 " (French → English) :

syndrome de microdélétion 16p13.11

Monosomy 16p13.11
SNOMEDCT-BE (disorder) / 719577000
SNOMEDCT-BE (disorder) / 719577000


syndrome de microduplication 16p13.3

Distal trisomy 16p
SNOMEDCT-BE (disorder) / 733473000
SNOMEDCT-BE (disorder) / 733473000


syndrome de microduplication 16p13.11

A recently described syndrome associated with variable clinical features including behavioral abnormalities, developmental delay, congenital heart defects and skeletal anomalies. This syndrome is caused by interstitial duplications encompassing 16p13
SNOMEDCT-BE (disorder) / 719578005
SNOMEDCT-BE (disorder) / 719578005




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syndrome de microdélétion 16p13

Date index:2023-05-15 -

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