-
1
-
-
0025364769
-
Isolation of fetal DNA from nucleated erythrocytes in maternal blood
-
Bianchi DW, Flint AF, Pizzimenti MF, Knoll JH, Latt SA (1990) Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proc Natl Acad Sci USA 87:3279-3283
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 3279-3283
-
-
Bianchi, D.W.1
Flint, A.F.2
Pizzimenti, M.F.3
Knoll, J.H.4
Latt, S.A.5
-
2
-
-
0020575533
-
Monoclonal antiglycophorin as a probe for erythroleukemias
-
Greaves MF, Sieff C, Edwards PA (1983) Monoclonal antiglycophorin as a probe for erythroleukemias. Blood 61:645-651
-
(1983)
Blood
, vol.61
, pp. 645-651
-
-
Greaves, M.F.1
Sieff, C.2
Edwards, P.A.3
-
4
-
-
0023158748
-
Flow cytometric analysis of human bone marrow. I. Normal erythroid development
-
Loken MR, Shah VO, Dattilio KL, Civin CI (1987) Flow cytometric analysis of human bone marrow. I. Normal erythroid development. Blood 69:255-263
-
(1987)
Blood
, vol.69
, pp. 255-263
-
-
Loken, M.R.1
Shah, V.O.2
Dattilio, K.L.3
Civin, C.I.4
-
5
-
-
0027288903
-
The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm
-
Reyniers E, Vits L, De Boulle K, Roy B van, Velzen D van, Graaf E de, Verkerk AJMH, Jorens HZJ, Darby JK, Oostra B, Willems PJ (1993) The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm. Nat Genet 4:143-148
-
(1993)
Nat Genet
, vol.4
, pp. 143-148
-
-
Reyniers, E.1
Vits, L.2
De Boulle, K.3
Van Roy, B.4
Van Velzen, D.5
De Graaf, E.6
Verkerk, A.J.M.H.7
Jorens, H.Z.J.8
Darby, J.K.9
Oostra, B.10
Willems, P.J.11
-
7
-
-
0027236971
-
Characterization and localisation of the FMR1 gene product associated with the fragile X syndrome
-
Verheij C, Bakker CE, Graaf E de, Keulemans J, Willemsen R, Verkerk AJMH, Galjaard H, Reuser AJJ, Hoogeveen AT, Oostra BA (1993) Characterization and localisation of the FMR1 gene product associated with the fragile X syndrome. Nature 363:722-724
-
(1993)
Nature
, vol.363
, pp. 722-724
-
-
Verheij, C.1
Bakker, C.E.2
De Graaf, E.3
Keulemans, J.4
Willemsen, R.5
Verkerk, A.J.M.H.6
Galjaard, H.7
Reuser, A.J.J.8
Hoogeveen, A.T.9
Oostra, B.A.10
-
8
-
-
0029063222
-
Characterization of FMR1 proteins isolated from different tissues
-
Verheij C, DeGraaff E, Bakker CE, Willemsen R, Willems PJ, Meijer N, Galjaard H, Reuser AJJ, Oostra BA, Hoogeveen AT (1995) Characterization of FMR1 proteins isolated from different tissues. Hum Mol Genet 4:895-901
-
(1995)
Hum Mol Genet
, vol.4
, pp. 895-901
-
-
Verheij, C.1
DeGraaff, E.2
Bakker, C.E.3
Willemsen, R.4
Willems, P.J.5
Meijer, N.6
Galjaard, H.7
Reuser, A.J.J.8
Oostra, B.A.9
Hoogeveen, A.T.10
-
9
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJMH, Pieretti M, Sutcliffe JS, Fu Y-H, Kuhl DPA, Pizutti A, Reiner O, Richards S, Victoria MF, Zhang F, Eussen BE, Ommen G-JB van, Blonden LAJ, Riggins GJ, Chastain JL, Kunst CB, Galjaard H, Caskey CT, Nelson DL, Oostra BA, Warren ST (1991) Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65:905-914
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhl, D.P.A.5
Pizutti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
Eussen, B.E.11
Van Ommen, G.-J.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
10
-
-
0029028295
-
Rapid antibody test for fragile X syndrome
-
Willemsen R, Mohkamsing S, De Vries B, Devys D, Ouweland A van de, Mandel JL, Galjaard H, Oostra B (1995) Rapid antibody test for fragile X syndrome. Lancet 345:1147-1148
-
(1995)
Lancet
, vol.345
, pp. 1147-1148
-
-
Willemsen, R.1
Mohkamsing, S.2
De Vries, B.3
Devys, D.4
Van De Ouweland, A.5
Mandel, J.L.6
Galjaard, H.7
Oostra, B.8
-
11
-
-
85046113287
-
Prenatal diagnosis of fragile X syndrome
-
Willemsen R, Oosterwijk JC, Los FJ, Galjaard H, Oostra BA (1996) Prenatal diagnosis of fragile X syndrome. Lancet 348: 967-968
-
(1996)
Lancet
, vol.348
, pp. 967-968
-
-
Willemsen, R.1
Oosterwijk, J.C.2
Los, F.J.3
Galjaard, H.4
Oostra, B.A.5
-
12
-
-
0031020588
-
Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A novel appraisal
-
Willemsen R, Los F, Mohkamsing S, van-den-Ouweland A, Deelen W, Galjaard H, Oostra B (1997) Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: a novel appraisal. J Med Genet 34:250-252
-
(1997)
J Med Genet
, vol.34
, pp. 250-252
-
-
Willemsen, R.1
Los, F.2
Mohkamsing, S.3
Van-Den-Ouweland, A.4
Deelen, W.5
Galjaard, H.6
Oostra, B.7
|