302 results on '"Cram, David S."'
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2. Variant haplophasing by long-read sequencing: a new approach to preimplantation genetic testing workups
3. Molecular testing for H. pylori clarithromycin and quinolone resistance: a prospective Chinese study
4. The uncertainty of copy number variants: pregnancy decisions and clinical follow-up
5. Third-generation sequencing: any future opportunities for PGT?
6. Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants
7. Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
8. Genetic profiling of primary and secondary tumors from patients with lung adenocarcinoma and bone metastases reveals targeted therapy options
9. Evaluation of multiplex ARMS-PCR for detection of Helicobacter pylori mutations conferring resistance to clarithromycin and levofloxacin
10. A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism
11. The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos
12. Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations
13. Molecular analysis of DNA in blastocoele fluid using next-generation sequencing
14. PGT‐A: The biology and hidden failures of randomized control trials
15. Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid
16. Expression of glutamic acid decarboxylase (GAD) and its role as an autoantigen in insulin-dependent diabetes
17. Cell-free DNA test for pathogenic copy number variations: A retrospective study
18. Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing
19. Detection and quantitation of chromosomal mosaicism in human blastocysts using copy number variation sequencing
20. IVF embryo choices and pregnancy outcomes
21. A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA)
22. Cloning from the Thyroid of a Protein Related to Actin Binding Protein that is Recognized by Graves Disease Immunoglobulins
23. A Hydrogenase-Linked Gene in Methanobacterium thermoautotrophicum Strain Δ H Encodes a Polyferredoxin
24. The potential of expanded noninvasive prenatal screening for detection of microdeletion and microduplication syndromes
25. Additional file 1 of Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants
26. Additional file 3 of Genetic profiling of primary and secondary tumors from patients with lung adenocarcinoma and bone metastases reveals targeted therapy options
27. A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples
28. Third-generation sequencing: any future opportunities for PGT?
29. REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis
30. Long-Molecule Sequencing
31. Analysis of balanced reciprocal translocations in patients with subfertility using single-molecule optical mapping
32. Single-Molecule Sequencing
33. Novel strategy with potential to identify developmentally competent IVF blastocysts
34. Gene expression profiling of human oocytes following in vivo or in vitro maturation
35. Genotyping of Rhesus SCNT pluripotent stem cell lines
36. Transcervical cell sampling: a need for clear terminology
37. DNA identification of fetal cells isolated from cervical mucus: potential for early non-invasive prenatal diagnosis
38. Inverse relation between humoral and cellular immunity to glutamic acid decarboxylase in subjects at risk of insulin-dependent diabetes
39. Laminin-1 Promotes Differentiation of Fetal Mouse Pancreatic beta-Cells
40. Isobaric tag for relative and absolute quantitation based quantitative proteomics reveals unique urinary protein profiles in patients with preeclampsia
41. Clinical application of single‐molecule optical mapping to a multigeneration FSHD1 pedigree
42. Transgenic Expression of Mouse Proinsulin II Prevents Diabetes in Nonobese Diabetic Mice
43. Antibodies to synovial antigens in recent-onset rheumatoid arthritis
44. Transcription factor jun-B is target of autoreactive T-cells in IDDM
45. An ELISA for antibodies to recombinant glutamic acid decarboxylase in IDDM
46. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing
47. High levels of circulating cell-free DNA are a biomarker of active SLE
48. Non-invasive prenatal testing of pregnancies at risk for phenylketonuria
49. A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
50. Divergence of Methanogens, Conservation of the His I Gene Sequence in all Three Biological Kingdoms and the Status of Methanobacterium Thermoautotrophicum
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