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Browsing by Author Osborne, LR
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Showing results 4 to 7 of 7
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Title
Author(s)
Issue Date
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor
Osborne, LR
Soder, S
Shi, XM
Pober, B
Costa, T
Scherer, SW
Tsui, L-C
1997
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome
Journal:
Genomics
Osborne, LR
Campbell, T
Daradich, A
Scherer, SW
Tsui, LC
1999
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients
Journal:
Genomics
Osborne, LR
Martindale, D
Scherer, SW
Shi, XM
Huizenga, J
Heng, HHQ
Costa, T
Pober, B
Lew, L
Brinkman, J
Rommens, J
Koop, B
Tsui, LC
1996
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7
Journal:
Genomics
Osborne, LR
Herbrick, JA
Greavette, T
Heng, HHQ
Tsui, LC
Scherer, SW
1997