16 results on '"Laissue, Paul"'
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2. Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing
3. Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms
4. ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure
5. Novel Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms
6. The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
7. Improving the evaluation of milestones for students completing a clinical genetics elective
8. Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing
9. Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations
10. BMP15 c.-9C>G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure
11. Polymorphisms of Human Placental Alkaline Phosphatase Are Associated with in Vitro Fertilization Success and Recurrent Pregnancy Loss
12. A novel familial case of diffuse leukodystrophy related to NDUFV1 compound heterozygous mutations
13. CITED2 mutations potentially cause idiopathic premature ovarian failure
14. Screening for mutations of the FOXO4 gene in premature ovarian failure patients
15. Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype
16. Recent advances in the study of genes involved in non-syndromic premature ovarian failure
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