Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3
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Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3
description
scientific article published on 07 January 2019
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wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2019
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name
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@en
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@nl
type
label
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@en
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@nl
prefLabel
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@en
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@nl
P2093
P1433
P1476
Association of GNAS imprinting ...... oparathyroidism type 1B/iPPSD3
@en
P2093
A Linglart
D Tessaris
G Mantovani
L deSanctis
M A Maffini
P Bordogna
P2888
P356
10.1186/S13148-018-0607-8
P407
P577
2019-01-07T00:00:00Z
P6179
1111225192