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Issue Date
Title
Author(s)
1997
FMR2 expression in families with FRAXE mental retardation
Gecz, J.
;
Oostra, B.
;
Hockey, A.
;
Carbonell, P.
;
Turner, G.
;
Haan, E.
;
Sutherland, G.
;
Mulley, J.
1995
A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
Laing, N.
;
Wilton, S.
;
Akkari, P.
;
Dorosz, S.
;
Boundy, K.
;
Kneebone, C.
;
Blumbergs, P.
;
White, S.
;
Watkins, H.
;
Love, D.
;
Haan, E.
1995
Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (∆F508)
Cui, K.H.
;
Haan, E.
;
Wang, L.J.
;
Matthews, C.
1996
Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome: implications for mapping and cloning the BOR gene
Gu, J.
;
Wagner, M.
;
Haan, E.
;
Wells, D.
Discover
Author
1
Akkari, P.
1
Blumbergs, P.
1
Boundy, K.
1
Carbonell, P.
1
Cui, K.H.
1
Dorosz, S.
1
Gecz, J.
1
Gu, J.
1
Hockey, A.
1
Kneebone, C.
.
next >
Subject
4
Humans
4
Molecular Sequence Data
3
Female
3
Sequence Deletion
2
DNA
2
Male
2
Membrane Proteins
2
Polymerase Chain Reaction
2
Polymorphism, Genetic
1
Abnormalities, Multiple
.
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Date issued
1
1997
1
1996
2
1995