Detalles de la búsqueda
1.
Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis.
J Med Genet
; 52(2): 95-103, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25515069
2.
Application value of CNV-seq for the prenatal diagnosis of women with high-risk pregnancies / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 17-20, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-970870
3.
Clinical phenotype and genetic analysis of twelve children with ring chromosomes / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 191-194, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-970903
4.
Value of high throughput sequencing in noninvasive prenatal screening / 实用医学杂志
The Journal of Practical Medicine
; (24): 433-436, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-743748
5.
Establishment and application of reference ranges of thyroid function in relation to pregnancy in Hubei / 中华地方病学杂志
Chinese Journal of Endemiology
; (12): 189-192, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-744279
6.
Cytogenetic analysis on 5329 children in genetic counseling / 实用医学杂志
The Journal of Practical Medicine
; (24): 479-482, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-743759
7.
Establishment of reference range of serum thyroid hormone in women with different gestational age in Wu-han area / 实用医学杂志
The Journal of Practical Medicine
; (24): 4082-4086, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-665452
8.
Analysis of the Mutations in SLC26A4 Gene in Children with Non-syndromic Hearing Loss / 听力学及言语疾病杂志
Journal of Audiology and Speech Pathology
; (6): 456-459, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-441448
Resultados
1 -
8
de 8
1
Próxima >
>>