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Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: A case series

โœ Scribed by Naomi Yachelevich; Julia Klein Gittler; Susan Klugman; Barbara Feldman; Joanna Martin; Susan Sklower Brooks; Carl Dobkin; Sarah L. Nolin


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
365 KB
Volume
155
Category
Article
ISSN
1552-4825

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Terminal deletion of the long arm of chr
โœ Petersen, Birgit; Strassburg, Hans-Michael; Feichtinger, Wolfgang; Kress, Wolfra ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 8 KB ๐Ÿ‘ 2 views

Since the first patient with partial deletion of the long arm of chromosome 10 was described in 1978, another 23 cases have been reported, with the breakpoint ranging from 10q23.3-26.2. To contribute further to the delineation of the monosomy 10qter syndrome, we describe a female child who, at age 3