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Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome
by
MCCONKIE-ROSELL, A
,
LACHIEWICZ, A. M
,
SPIRIDIGLIOZZI, G. A
,
TARLETON, J
,
SCHOENWALD, S
,
PHELAN, M. C
,
PONMANI GOONEWARDENA
,
XIAOHUA DING
,
BROWN, W. T
Published in
American journal of human genetics
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Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B
by
Michaelis, R.C.
,
Velagaleti, G.V.N.
,
Jones, C.
,
Pivnick, E.K.
,
Phelan, M.C.
,
Boyd, E.
,
Tarleton, J.
,
Wilroy, R.S.
,
Tunnacliffe, A.
,
Tharapel, A.T.
Published in
American journal of medical genetics
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Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B
by
Michaelis, R.C.
,
Velagaleti, G.V.N.
,
Jones, C.
,
Pivnick, E.K.
,
Phelan, M.C.
,
Boyd, E.
,
Tarleton, J.
,
Wilroy, R.S.
,
Tunnacliffe, A.
,
Tharapel, A.T.
Published in
American journal of medical genetics
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A Companion to Narrative Theory
by
Phelan, James
,
Rabinowitz, Peter J
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Reference Reviews
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Chromosome Fragility
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