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Human Genetics|November 1, 1987
Linkage relationships of X-linked choroideremia to DXYS1 and DXS3I M MacDonald, R M Sandre, P Wong, et al.
American Journal of Medical Genetics|February 5, 1998
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sexT Costa, M Lambert, I Teshima, et al.
American Journal of Medical Genetics|February 1, 1988
A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndromeS Wood, R J Shukin, B C McGillivray, et al.
Clinical Performance and Quality Health Care|February 24, 2001
Assessment of health status at two years of very low birthweight infants--clinical governanceP Stutchfield, S Nicklin, P Minchom, et al.
Frontiers in Bioengineering and Biotechnology|December 7, 2020
Mechanical Characterization for Cellular Mechanobiology: Current Trends and Future ProspectsBadri Narayanan Narasimhan, Matthew S Ting, Tarek Kollmetz, et al.
Ophthalmology|October 1, 1998
A practical diagnostic test for choroideremiaI M MacDonald, D Y Mah, Y K Ho, et al.
Neuromuscular Disorders : NMD|March 29, 2000
Expression and synthesis of alternatively spliced variants of Dp71 in adult human brainR C Austin, G E Morris, P L Howard, et al.
American Journal of Human Genetics|April 1, 1990
Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlationX Y Hu, P N Ray, E G Murphy, et al.
Gene|August 1, 1989
Fine structure analysis of the Chinese hamster AS gene encoding asparagine synthetaseI L Andrulis, M Shotwell, S Evans-Blackler, et al.
Diabetes Technology & Therapeutics|July 27, 2001
Tele-ophthalmology via stereoscopic digital imaging: a pilot projectM T Tennant, C J Rudnisky, B J Hinz, et al.
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