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Cancer Genetics and Cytogenetics|July 1, 1991
der(3)t(3;5). Another recurring abnormality in myelodysplastic disorderV Lindgren, L Gibson, T L Yang-Feng
American Journal of Medical Genetics|June 1, 1990
Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2])C R Bryke, V Lindgren, J S Fryburg, et al.
American Journal of Human Genetics|September 1, 1992
Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndromeK Y Gandelman, L Gibson, M S Meyn, et al.
Human Genetics|February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypesV Lindgren, C P Chen, C R Bryke, et al.
American Journal of Medical Genetics|August 1, 1994
FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotypeT W Chu, A S Teebi, L Gibson, et al.
Genomics|February 1, 1988
Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genesT L Yang-Feng, J W Schneider, V Lindgren, et al.
American Journal of Medical Genetics|May 15, 1993
Molecular and cytogenetic characterization of 9p- abnormalitiesA S Teebi, L Gibson, J McGrath, et al.
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