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1.
A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [ß7(A4)GluâLys; HBB: c.22G>A] and Hb H Disease.
Hemoglobin
; 46(6): 338-340, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-36691989
2.
Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy.
Clin Chem Lab Med
; 55(3): 358-367, 2017 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27754957
3.
Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls.
BMC Musculoskelet Disord
; 16: 11, 2015 Feb 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-25888055
4.
[Association Analysis between Genotype and Phenotype of α,ß-Thalassaemia Carriers in Huizhou Area of Guangdong Province].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 31(4): 1133-1137, 2023 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-37551488
5.
A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction.
Anal Biochem
; 427(2): 144-50, 2012 Aug 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22617799
6.
Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study.
Taiwan J Obstet Gynecol
; 60(4): 763-765, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-34247821
7.
Impact of the CYP3A5, CYP3A4, COMT, IL-10 and POR genetic polymorphisms on tacrolimus metabolism in Chinese renal transplant recipients.
PLoS One
; 9(1): e86206, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24465960
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