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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.
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.
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.
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