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Cytogenetics and Cell Genetics|January 1, 1991
Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping, banding, and investigation of sequence organizationJ Gosden, D Hanratty, J Starling, et al.Journal of Medical Genetics|August 25, 2005
Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twinsD Johnson, N Morrison, L Grant, et al.Nature Genetics|March 1, 1996
CpG islands of chicken are concentrated on microchromosomesH A McQueen, J Fantes, S H Cross, et al.British Journal of Haematology|May 1, 1994
Trisomy 12 in B-cell chronic lymphocytic leukaemia: assessment of lineage restriction by simultaneous analysis of immunophenotype and genotype in interphase cells by fluorescence in situ hybridizationJ Garcìa-Marco, E Matutes, R Morilla, et al.Human Genetics|April 1, 1992
Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndromeA M Sharkey, L McLaren, M Carroll, et al.Journal of Medical Genetics|March 1, 1997
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locusJ A Crolla, J E Cawdery, C A Oley, et al.Human Molecular Genetics|March 1, 1995
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotypeJ Fantes, B Redeker, M Breen, et al.Genomics|June 1, 1997
The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouseJ Kent, M Lee, A Schedl, et al.Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.Human Molecular Genetics|February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IK L Evans, J Fantes, C Simpson, et al.Pageof 3