257 results on '"Khan, P. Meera"'
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2. DNA Diagnosis in Families with Hereditary Forms of Cancer
3. Linkage Studies on Familial Adenomatous Polyposis in the Netherlands
4. Assignment of the AK 1 :Np:ABO Linkage Group to Human Chromosome 9
5. A Targeted Chain-Termination Mutation in the Mouse Apc Gene Results in Multiple Intestinal Tumors
6. Complete Structure of the α B-Crystallin Gene: Conservation of the Exon--Intron Distribution in the Two Nonlinked α -Crystallin Genes
7. Human Antigen and Enzyme Markers in Man-Chinese Hamster Somatic Cell Hybrids: Evidence for Synteny between the HL-A, PGM 3 , ME 1 , and IPO-B Loci
8. Mitotic Separation of Two Human X-Linked Genes in Man--Mouse Somatic Cell Hybrids
9. Summary of Chapter 6: Cytomolecular Aspects of Polyposis
10. Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development
11. Germline mutations in the 3′ part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli
12. Multiple products in the protein truncation test due to alternative splicing in the adenomatous polyposis coli (APC) gene
13. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
14. APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis
15. Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer
16. Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis
17. Paternal duplication of chromosome 5q11.2–5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies
18. Surveillance in hereditary nonpolyposis colorectal cancer: An international cooperative study of 165 families
19. A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis
20. Human αB-crystallin (CRYA2) gene mapped to chromosome 11q12-q23
21. [6]Protein truncation test for presymptomatic diagnosis of familial adenomatous polyposis
22. Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3[prime] APC mutation
23. A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers
24. Molecular genetic tests as a guide to surgical management of familial adenomatous polyposis
25. A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines
26. Interval cancers in hereditary non-polyposis colorectal cancer (Lynch syndrome)
27. Screening for hereditary colorectal cancer
28. Molecular Basis and Enzymatic Properties of Glucose 6-Phosphate Dehydrogenase Volendam, Leading to Chronic Nonspherocytic Anemia, Granulocyte Dysfunction, and Increased Susceptibility to Infections
29. A Search for Associations between Genetical Polymorphic Systems and Physical, Biochemical and Haematological Variables
30. Gene Frequencies in a Dutch Population
31. Genetical Studies on the Multiple Forms of Human Guanylate Kinase in Man-Chinese Hamster Somatic Cell Hybrids
32. Search for Genetic Markers Associated with Crohn’s Disease in the Netherlands
33. Adenosine Deaminase (ADA; E.C. no. 3.5.4.4.) in Colorectal Adenocarcinoma in Man
34. Adenosine Deaminase Isozymes in Transformed Cells
35. Basic Molecular Defect in ADA SCID
36. Cell Surface Adenosine Deaminase (ADA) and its Complexing Protein (ADCP) in Human T-Lymphoid Cells
37. Gluten Sensitive Enteropathy in Spain: Genetic and Environmental Factors
38. A Study of Andhra Marriages Consanguinity, Caste, Illiteracy, and Bridal Age
39. A New Variant Allele AK₅ of the Red Cell Adenylatekinase Polymorphism in a Non-Tribal Indian Population
40. Assignment of the catechol-O-methyltransferase gene to human chromosome 22 in somatic cell hybrids
41. The human PGM-2 and its chromosomal localization in man-mouse hybrids
42. The distribution of esterase D variants in different ethnic groups
43. Assignment of adenosine deaminase complexing protein (ADCP) gene(s) to human chromosome 2 in rodent-human somatic cell hybrids
44. Prevalence and molecular heterogeneity of alfa+thalassemia in two tribal populations from Andhra Pradesh, India
45. Localization of HLA on the short arm of chromosome 6
46. Rapid detection of glyoxalase I (GLO) on cellulose acetate gel and the distribution of GLO variants in a Dutch population
47. A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids
48. Mapping SB in relation to HLA and GL01 using cells from first-cousin marriage offspring
49. Catechol-O-methyltransferase: A method for autoradiographic visualization of isozymes in Cellogel
50. Immunohistochemical localization of adenosine deaminase complexing protein in intestinal mucosa and in colorectal adenocarcinoma as a marker for tumour cell heterogeneity
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