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- Q90025168 description "artículu científicu espublizáu en mayu de 2019" @default.
- Q90025168 description "scientific article published on 01 May 2019" @default.
- Q90025168 description "wetenschappelijk artikel" @default.
- Q90025168 description "наукова стаття, опублікована 1 травня 2019" @default.
- Q90025168 name "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
- Q90025168 name "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
- Q90025168 type Item @default.
- Q90025168 label "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
- Q90025168 label "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
- Q90025168 prefLabel "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
- Q90025168 prefLabel "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
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- Q90025168 P1476 Q90025168-660DEB00-338E-45BE-9FAB-AFD94F2572D0 @default.
- Q90025168 P2093 Q90025168-277A1C28-BE02-4CF8-B3ED-CB25BDBDBF6D @default.
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- Q90025168 P31 Q90025168-00149D4D-7C33-43B9-85A2-D18CA9061759 @default.
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- Q90025168 P921 Q90025168-BA1AF7D2-EC31-4CE2-8391-D168D9DECFFB @default.
- Q90025168 P356 0970-258X.278692 @default.
- Q90025168 P698 32129306 @default.
- Q90025168 P1433 Q7753202 @default.
- Q90025168 P1476 "Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India" @default.
- Q90025168 P2093 "Anna Simon" @default.
- Q90025168 P2093 "Sarah Mathai" @default.
- Q90025168 P2093 "Sony Mohan" @default.
- Q90025168 P2093 "Sumita Danda" @default.
- Q90025168 P304 "141-143" @default.
- Q90025168 P31 Q13442814 @default.
- Q90025168 P356 "10.4103/0970-258X.278692" @default.
- Q90025168 P433 "3" @default.
- Q90025168 P478 "32" @default.
- Q90025168 P577 "2019-05-01T00:00:00Z" @default.
- Q90025168 P698 "32129306" @default.
- Q90025168 P921 Q30990102 @default.
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