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American Journal of Medical Genetics|December 30, 1996
SPONASTRIME dysplasia: report on a female patient with severe skeletal changesM Masuno, G Nishimura, M Adachi, et al.
American Journal of Medical Genetics|December 1, 1994
Submicroscopic deletion of chromosome region 16p13.3 in a Japanese patient with Rubinstein-Taybi syndromeM Masuno, K Imaizumi, K Kurosawa, et al.
No to Hattatsu = Brain and Development|August 8, 1998
[Three Japanese children with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)]T Wada, M Nakamura, Y Matsushita, et al.
Human Genetics|March 10, 1999
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCRT Kubota, S Nonoyama, H Tonoki, et al.
American Journal of Medical Genetics|October 23, 1997
Another critical region for deletion of 22q11: a study of 100 patientsH Kurahashi, E Tsuda, R Kohama, et al.
Clinical Genetics|June 4, 1998
Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivationK Sukegawa, T Matsuzaki, S Fukuda, et al.
American Journal of Medical Genetics|October 1, 1991
Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocationM Masuno, Y Cholsong, T Kuwahara, et al.
Genes, Chromosomes & Cancer|April 30, 1999
Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: molecular analysis in four patientsK Muroya, T Ishii, Y Nakahori, et al.
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