59 results on '"van Heyningen, V."'
Search Results
2. Wilms’ Tumour ’ A Developmental Anomaly
3. SELECTION OF MONOCLONAL ANTIBODIES FOR DESIGNATED USES
4. Molecular Analysis of the Aniridia — Wilms’ Tumor Syndrome
5. TOWARD ANALYSIS OF THE HLA-DR SYSTEM WITH MONOCLONAL ANTIBODIES
6. MITOCHONDRIAL ENZYMES IN MAN-MOUSE HYBRID CELLS
7. Monoclonal Anti-B Cell Antibodies: their Effects on Human Mixed Lymphocyte Reactions
8. Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes
9. FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality
10. FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality
11. Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2
12. Mechanisms of non-Mendelian inheritance in genetic disease
13. Cognitive functioning in humans with mutations of the PAX6 gene
14. PAX6 in sensory development
15. PAX6mutation in a family with aniridia, congenital ptosis, and mental retardation
16. Hemolytic uremic syndrome associated with Denys-Drash syndrome
17. Role of Pax6 in development of the cerebellar system
18. Psychiatric disorder and cognitive function in a family with an inherited, novel mutation of the developmental control gene PAX6
19. Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998
20. In utero nephropathy, Denys-Drash syndrome and Potter phenotype
21. Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: Dose effect of the PAX6 gene product?
22. Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations
23. Pax6 Controls Progenitor Cell Identity and Neuronal Fate in Response to Graded Shh Signaling
24. The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.
25. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
26. A new PAX6 mutation in familial aniridia.
27. Do children with diffuse mesangial sclerosis in association with mutations of the Wilms' tumour suppressor gene (WT1) require bilateral nephrectomy?
28. Micronucleus frequencies in lymphoblastoid cell lines measured with the cytokinesis-block technique and flow cytometry
29. Assignment of 112 Microsatellite Markers to 23 Chromosome 11 Subregions Delineated by Somatic Hybrids: Comparison with the Genetic Map
30. Reassessment of breakpoints in chromosome 11p15
31. HumanRAG2, likeRAGI, is on chromosome II band p13 and therefore not linked to ataxia telangiectasia complementation groups
32. Modulation of DNA Binding Specificity by Alternative Splicing of the Wilms Tumor wt1 Gene Transcript
33. Zinc finger point mutations within the WT1 gene in Wilms tumor patients.
34. Report of the Second Chromosome 11 Workshop
35. High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered
36. Cultured epithelial cells from patients with Cystic Fibrosis have an increased expression of the 14 kDa Ca2+-binding protein CFA
37. Report of the committee on the genetic constitution of chromosome 11
38. Related calcium-binding proteins map to the same subregion of chromosome 1q and to an extended region of synteny on mouse chromosome 3
39. Role for the Wilms tumor gene in genital development?
40. Report of the committee on the genetic constitution of chromosome 11
41. Development and utility of a monoclonal-antibody-based, highly sensitive immunoradiometric assay of thyrotropin.
42. Association between pregnancy-associatedα 2-glycoprotein (α 2-PAG) and mixed leucocyte reaction determinants on the leucocyte surface
43. Clinical Value of Imaging Using Antibody to Alpha Fetoprotein in Germ Cell Tumours
44. Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.)
45. Assignment of the genes for mitochondrial malate dehydrogenase and for SV40 T-antigen to human chromosome 7
46. Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13
47. The β2-microglobulin gene is on chromosome 15 and not in the HL-A region
48. Linkage relationships of the HL-A system and β2 microglobulin
49. Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
50. Assignment of the genes for human mitochondrial malate dehydiogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybrids
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.