Samuel J H Parsons

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0CO-AUTHORS
Developmental genetics (incl. sex determination)
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Publications (1)

|Jun 07, 2017
A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.

Samuel J H Parsons, Neville B Wright, Emma Burkitt-Wright

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