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American Journal of Human Genetics|March 1, 1990
Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisH Nakase, C T Moraes, R Rizzuto, et al.
American Journal of Human Genetics|February 1, 1990
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markersC R Greenberg, J A Evans, S McKendry-Smith, et al.
American Journal of Human Genetics|November 1, 1991
Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patientsD Stoppa-Lyonnet, C Duponchel, T Meo, et al.
American Journal of Human Genetics|August 1, 1992
Strategies for characterizing highly polymorphic markers in human gene mappingJ Ott
American Journal of Human Genetics|August 1, 1992
Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiencyA L Jørgensen, J Philip, W H Raskind, et al.
American Journal of Human Genetics|August 1, 1992
Segregation analysis of cancer in families of childhood soft-tissue-sarcoma patientsE D Lustbader, W R Williams, M L Bondy, et al.
American Journal of Human Genetics|August 1, 1992
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumM Sarfarazi, C Wijmenga, M Upadhyaya, et al.
American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.
American Journal of Human Genetics|August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35B Weiffenbach, R Bagley, K Falls, et al.
American Journal of Human Genetics|August 1, 1992
Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35K D Mathews, K A Mills, E P Bosch, et al.
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