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Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing.
Arch Endocrinol Metab
; 61(6): 633-636, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29412390
2.
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
Arch. endocrinol. metab. (Online)
; 61(6): 633-636, Dec. 2017. graf
Artículo
en Inglés
| LILACS | ID: biblio-887602
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