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L. C. Fairbrother
L. C. Fairbrother
Arthrogryposis
Breakpoint
Microdeletion syndrome
Neurological findings
Phenotype
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Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?
2014
Case reports in genetics
K. M. Usrey
C. A. Williams
M Dasouki
L. C. Fairbrother
Merlin G. Butler
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Citations (13)
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