1,398 results on '"Simpson, Joe Leigh"'
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2. Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research.
3. Enabling precision medicine in neonatology, an integrated repository for preterm birth research.
4. Clinical Outcome of Preimplantation Genetic Testing
5. Social, Ethical, and Legal Aspects
6. Origin of Aneuploidy and Strategies Underlying Clinical Application of Preimplantation Genetic Testing for Chromosomal Disorders (PGT-A and PGT-SR)
7. Preimplantation Genetic Testing (PGT) for Human Leukocyte Antigens (HLA) (PGT-HLA)
8. Strategies and Indications for Preimplantation Genetic Testing for Monogenic Disorders (PGT-M)
9. Major Components of Preimplantation Genetic Testing: Adjustment of Available Genetic Technology to PGT Practice
10. Place of Preimplantation Genetic Testing (PGT) Among Available Options for Prevention of Genetic Disorders
11. The Genetic Risk of a Couple Aiming to Conceive
12. Risky Business: Meeting the Structural Needs of Transdisciplinary Science
13. LIST OF Contributors
14. Hypogonadotropic and Hypergonadotropic Hypogonadism in Females: Disorders of Reproductive Ducts
15. Before the beginning: the genetic risk of a couple aiming to conceive
16. Prenatal genetic testing and treatment for congenital adrenal hyperplasia
17. Preimplantation Genetic Testing in the Future
18. The Genetics of Spontaneous Abortions
19. Forty years of IVF
20. Practical Preimplantation Genetic Testing
21. Preimplantation diagnosis and other modern methods for prenatal diagnosis
22. Preimplantation Genetic Screening and Diagnostic Testing
23. Contributors
24. Prenatal Diagnosis and Treatment of Genetic Steroid Disorders
25. Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders
26. Contributors
27. Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction
28. Reproducing Genetics
29. Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete müllerian fusion
30. Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency
31. Birth defects and assisted reproductive technologies
32. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure
33. Can Pregnancies Be Achieved in Premature Ovarian Insufficiency?
34. 33 - Aborto
35. 10 - Cribado y diagnóstico genético
36. Chapter 4B - Contemporary prenatal genetic diagnosis for congenital adrenal hyperplasia: preimplantation genetic testing and maternal cell-free DNA
37. Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status
38. Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index
39. Risky Business: Meeting the Structural Needs of Transdisciplinary Science
40. The International Glossary on Infertility and Fertility Care, 2017
41. Preimplantation genetic diagnosis to improve pregnancy outcomes in subfertility
42. Preface
43. Contributors
44. Early Pregnancy Loss and Stillbirth
45. Genetics of Premature Ovarian Failure: New Developments in Etiology
46. Genetic Screening and Prenatal Genetic Diagnosis
47. Dedication
48. Invasive procedures for prenatal diagnosis: Any future left?
49. The Illusory "Level Playing Field" [with reply]
50. Genetics of Oocyte Depletion
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