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Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern

D. J. Wolff; Karen M. Gustashaw; Vickie Zurcher; Lara Ko; Wendy White; Lester Weiss; Daniel L. Van Dyke; Stuart Schwartz; Huntington F. Willard
Human Genetics · Vol. 100, Issue 2 · pp. 256-262 · 1997
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date1997-07-09
Publication Year1997
Volume100
Issue2
Pages256-262
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s004390050501

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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