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1.
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing.
Hemoglobin
; 46(3): 160-163, 2022 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-35582759
2.
[Serum level of soluble transferrin receptor in children with hemoglobin H disease].
Zhongguo Dang Dai Er Ke Za Zhi
; 21(9): 894-897, 2019 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-31506149
3.
Detecting rare thalassemia in children with anemia using third-generation sequencing.
Hematology
; 28(1): 2241226, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-37548329
4.
[Application Value of Capillary Electrophoresis in Screeningß-Thalassemia of Children].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 28(1): 230-234, 2020 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-32027282
5.
[Genotypic and Phenotypic Analysis of αß-Thalassemia in Children].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 27(4): 1232-1235, 2019 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-31418385
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