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; Mars S. Skae; Phillip G. Murray
Author Information: Manchester Academic Health Sciences Centre, Centre for Paediatrics and Child Health, Institute of Human Development
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