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Samuel J H Parsons
Samuel J H Parsons
Item
http://www.wikidata.org/entity/Q96249351
Q96249351
about
A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.
P50
Q52092392-ED658622-07CB-4933-AA57-F158E860FC12
P50
Samuel J H Parsons
Item
http://www.wikidata.org/entity/Q96249351
description
wetenschapper
@nl
name
Samuel J H Parsons
@en
Samuel J H Parsons
@nl
type
Item
label
Samuel J H Parsons
@en
Samuel J H Parsons
@nl
prefLabel
Samuel J H Parsons
@en
Samuel J H Parsons
@nl
P31
Q96249351-139EB4B7-BED1-4505-8B06-611A0F9B8F84
P496
Q96249351-E924A1E2-40EA-40F8-8DD8-AD0D704FBCB5
P496
0000-0003-3008-8966
P31
Afgan
P496
0000-0003-3008-8966
http://www.w3.org/2001/XMLSchema#string