602 results on '"Andria, G"'
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2. Chromosomal, Gestational, and Neonatal Outcomes of Embryos Classified as Mosaic by Preimplantation Genetic Testing for Aneuploidy
3. Evidence-based management of preimplantation chromosomal mosaicism: lessons from the clinic
4. Using outcome data from one thousand mosaic embryo transfers to formulate an embryo ranking system for clinical use
5. Clinical error rates of next generation sequencing and array comparative genomic hybridization with single thawed euploid embryo transfer
6. Experiences and psychological outcomes of the oocyte donor: a survey of donors post-donation from one center
7. Transfer of embryos with positive results following preimplantation genetic testing for monogenic disorders (PGT-M): experience of two high-volume fertility clinics
8. Lack of evidence to support recommendation for prenatal uniparental disomy (UPD) analysis following mosaic embryo transfer
9. Errors in Genetic Testing: The Fourth Case Series
10. Characterization of Innovation Oil Level Sensors for Aerospace Application
11. Factors Affecting Recall of Different Types of Personal Genetic Information about Alzheimer’s Disease Risk : The REVEAL Study
12. CAN CHROMOSOME NUMBER PREDICT MOSAIC EMBRYO TRANSFER OUTCOME?
13. Geostatistical approach for validating contaminated soil measurements
14. BALANCING IT OUT: IN VITRO FERTILIZATION OUTCOMES AFTER PRE-IMPLANTATION GENETIC TESTING FOR CHROMOSOMAL STRUCTURAL REARRANGEMENTS AMONG CARRIERS OF ROBERTSONIAN AND RECIPROCAL TRANSLOCATIONS
15. ASSESSMENT FOR PREDICTORS OF EMBRYO PLOIDY FOLLOWING INCONCLUSIVE NEXT-GENERATION SEQUENCING (NGS)-BASED PREIMPLANTATION GENETIC TESTING FOR ANEUPLOIDY (PGT-A)
16. QUESTIONING THE BENEFIT OF REPORTING LOW LEVEL SEGMENTAL MOSAICISM: SIMILAR OBSERVED REPRODUCTIVE POTENTIAL COMPARED TO EUPLOID EMBRYOS
17. POST-DELIVERY CHROMOSOMAL ANALYSIS OF PLACENTAS ARISING FROM THE TRANSFER OF EMBRYOS DIAGNOSED AS MOSAIC
18. EXPANDING USE OF PREIMPLANTATION GENETIC TESTING FOR MONOGENIC DISORDERS (PGT-M) AMONG CARRIER COUPLES FOR CYSTIC FIBROSIS (CF)
19. Linear filtering of 2-D wavelet coefficients for denoising ultrasound medical images
20. Limited Antibody-Dependent Cellular Cytotoxicity Antibody Response Induced by a Herpes Simplex Virus Type 2 Subunit Vaccine
21. Contiguous Gene Syndromes Due to Deletions in the Distal Short Arm of the Human X Chromosome
22. Isolation and Characterization of a Steroid Sulfatase cDNA Clone: Genomic Deletions in Patients with X-chromosome-Linked Ichthyosis
23. Cervical Antibody Responses to a Herpes Simplex Virus Type 2 Glycoprotein Subunit Vaccine
24. Localization and Characterization of Cable Faults with TDR and Convolutional Neural Networks
25. DOUBLE EMBRYO TRANSFER (DET) WITH MOSAIC EMBRYOS HAVE EQUIVALENT LIVE BIRTH AND MULTIPLE PREGNANCY RATES AS EUPLOID DET
26. BLINDED REANALYSIS OF NEXT-GENERATION SEQUENCING (NGS) NON-EUPLOID EMBRYOS USING SINGLE NUCLEOTIDE POLYMORPHISM (SNP) ARRAY-BASED PRE-IMPLANTATION GENETIC TESTING FOR ANEUPLOIDY (PGT-A)
27. SINGLE THAWED NON-MOSAIC SEGMENTAL ANEUPLOID EMBRYO TRANSFER RESULTS IN ONGOING PREGNANCY AND NORMAL PRENATAL DIAGNOSIS
28. Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b
29. Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotype
30. Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders?
31. Accurate simultaneous measurement of heartbeat and respiratory intervals using a smartphone.
32. Upper airway obstructive disease in mucopolysaccharidoses: Polysomnography, computed tomography and nasal endoscopy findings
33. HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation
34. Vitamin D status in patients affected by Smith-Lemli-Opitz syndrome
35. The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: A position statement
36. Subclinical hypothyroidism and Down's syndrome; studies on myocardial structure and function
37. Chapter 6 - Genetic counseling for preimplantation genetic testing (PGT): Practical and ethical challenges
38. Clinical aspects of cystathionine β-synthase deficiency: how wide is the spectrum?
39. Phenylketonuria in Italy: Distinct distribution pattern of three mutations of the phenylalanine hydroxylase gene
40. Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionineβ-synthase mutations
41. Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations
42. Molecular analysis of patients affected by homocystinuria due to cystathionine β-synthase deficiency: report of a new mutation in exon 8 and a deletion in intron 11
43. Royal academy of medicine in Ireland international conference on homocysteine metabolism from basic science to clinical medicine: Proceedings of meeting held at Dromoland Castle, Co. Clare on July 2nd–6th, 1995
44. DIFFERENCES IN GENETIC CARRIER SCREENING (CS) PANELS NECESSITATE INTENDED PARENT (IP) EDUCATION FOR GAMETE DONOR SELECTION
45. Efficacy of ACE-inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study
46. Commentary
47. Linearization of A/D converters by dither and Chebyshev polynomials
48. Alström syndrome: intrafamilial phenotypic variability in sibs with a novel nonsense mutation of the ALMS1 gene
49. Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide
50. Down syndrome and breastfeeding
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