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1.
Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1.
Int J Mol Sci
; 21(22)2020 Nov 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-33202802
2.
Adaptation, reliability and validity of health-related quality of life questionnaires: Disabkids chronic and specific diabetes disease in children and adolescents with diabetes mellitus type 1.
Endocrinol Diabetes Nutr (Engl Ed)
; 70 Suppl 3: 18-26, 2023 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-37598007
3.
Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: atypical findings and a novel mutation in NR0B1.
J Pediatr Endocrinol Metab
; 28(9-10): 1129-37, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-26030781
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