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The Journal of Clinical Endocrinology and Metabolism|April 30, 2010
Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesisA Thorwarth, I Mueller, H Biebermann, et al.Transactions of the Ophthalmological Societies of the United Kingdom|January 1, 1986
Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysisM Warburg, U Friedrich, L Bleeker-Wagemakers, et al.Cytogenetics and Cell Genetics|January 1, 1997
Complex FISH probes for the subtelomeric regions of all human chromosomes: comparative hybridization of CEPH YACs to chromosomes of the Old World monkey Presbytis cristata and great apesK Kingsley, J Wirth, S van der Maarel, et al.Human Genetics|January 1, 1983
Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosomeP Wieacker, T F Wienker, B Dallapiccola, et al.Helvetica Paediatrica Acta|September 1, 1982
Adrenal insufficiency, myopathic hypotonia, severe psychomotor retardation, failure to thrive, constipation and bladder ectasia in 2 brothers: adrenomyodystrophyW von Petrykowski, R Beckmann, N Böhm, et al.Human Genetics|April 1, 1990
An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locusP M van Zandvoort, C A van Bennekom, H H Ropers, et al.Nucleic Acids Research|February 25, 1990
Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresisT J van de Pol, F P Cremers, R M Brohet, et al.Cytogenetic and Genome Research|August 12, 2005
Differences in the pattern of X-linked gene expression between fetal bovine muscle and fibroblast cultures derived from the same muscle biopsiesM I Nino-Soto, U A Nuber, P K Basrur, et al.Genome Research|May 18, 1999
Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1B Brunner, T Todt, S Lenzner, et al.Genomics|July 1, 1993
Physical mapping of DNA markers in the q13-q22 region of the human X chromosomeC Philippe, F P Cremers, M Chery, et al.Pageof 21