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1.
Isolated 17,20-Lyase Deficiency in a CYB5A Mutated Female With Normal Sexual Development and Fertility.
J Endocr Soc
; 4(2): bvz016, 2020 Feb 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32051920
2.
Contiguous gene deletion in a Chinese family with X-linked nephrogenic diabetes insipidus: challenges in early diagnosis and implications for affected families.
J Pediatr Endocrinol Metab
; 32(8): 915-920, 2019 Aug 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-31271558
3.
One amino acid makes a difference-Characterization of a new TPMT allele and the influence of SAM on TPMT stability.
Sci Rep
; 7: 46428, 2017 05 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-28462921
4.
Development of a broad toxicological screening technique for urine using ultra-performance liquid chromatography and time-of-flight mass spectrometry.
Anal Chim Acta
; 649(1): 80-90, 2009 Sep 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-19664466
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