-
2
-
-
0026713048
-
Birth of normal girl after in vitro fertilization and preimplantation diagnosis testing for cystic fibrosis
-
Handyside AH, Lesko JG, Tarin JJ, Winston RML, Hughes M: Birth of normal girl after in vitro fertilization and preimplantation diagnosis testing for cystic fibrosis. N Engl J Med 1992; 327:905-909
-
(1992)
N Engl J Med
, vol.327
, pp. 905-909
-
-
Handyside, A.H.1
Lesko, J.G.2
Tarin, J.J.3
Winston, R.M.L.4
Hughes, M.5
-
3
-
-
0031041689
-
Current status of preimplantation diagnosis
-
Verlinsky Y, Munne S, Simpson JL, Kuliev A, Ao A, Ray P, et al.: Current status of preimplantation diagnosis. J Assist Reprod Genet 1997;14(2):71-75
-
(1997)
J Assist Reprod Genet
, vol.14
, Issue.2
, pp. 71-75
-
-
Verlinsky, Y.1
Munne, S.2
Simpson, J.L.3
Kuliev, A.4
Ao, A.5
Ray, P.6
-
5
-
-
0030000924
-
Fluorescent polymerase chain reaction: Part I. A new method allowing genetic diagnosis allowing genetic diagnosis and DNA fingerprinting of single cells
-
Findlay I, Quirke P: Fluorescent polymerase chain reaction: Part I. A new method allowing genetic diagnosis allowing genetic diagnosis and DNA fingerprinting of single cells. Hum Reprod Update 1996;2(2):137-152
-
(1996)
Hum Reprod Update
, vol.2
, Issue.2
, pp. 137-152
-
-
Findlay, I.1
Quirke, P.2
-
6
-
-
0030022056
-
Reduced allele drop-out in single cell analysis for preimplantation genetic diagnosis of cystic fibrosis
-
Ray P, Winston R, Handyside A: Reduced allele drop-out in single cell analysis for preimplantation genetic diagnosis of cystic fibrosis. J Assist Reprod Genet 1996;13:104-106
-
(1996)
J Assist Reprod Genet
, vol.13
, pp. 104-106
-
-
Ray, P.1
Winston, R.2
Handyside, A.3
-
7
-
-
0028566231
-
Preimplantation diagnosis of genetic and chromosomal Diseases
-
Verlinsky Y, Handyside A, Grifo J, Munne S, Liebaers I, Levison G, Arnheim N, Hughes M, Delhanty J, et al.: Preimplantation diagnosis of genetic and chromosomal Diseases. J Assist Reprod Genet 1994;11:236-243
-
(1994)
J Assist Reprod Genet
, vol.11
, pp. 236-243
-
-
Verlinsky, Y.1
Handyside, A.2
Grifo, J.3
Munne, S.4
Liebaers, I.5
Levison, G.6
Arnheim, N.7
Hughes, M.8
Delhanty, J.9
-
8
-
-
0030020358
-
Preimplantation diagnosis of inherited disease by embryo biopsy
-
Harper J. Preimplantation diagnosis of inherited disease by embryo biopsy. J Assist Reprod Genet 1996;13:90-95
-
(1996)
J Assist Reprod Genet
, vol.13
, pp. 90-95
-
-
Harper, J.1
-
9
-
-
0026078815
-
A diomorphic 4-bp repeat in the cystic fibrosis gene is an absolute linkage disequilibrium with a delta f508 mutation: Implications for prenatal diagnosis and mutation origin
-
Chebab D, Johnson J, Louie E, Goossens M, Kawasaki E, Erlich H: A diomorphic 4-bp repeat in the cystic fibrosis gene is an absolute linkage disequilibrium with a delta f508 mutation: Implications for prenatal diagnosis and mutation origin. J Hum Genet 1991;48:223-226
-
(1991)
J Hum Genet
, vol.48
, pp. 223-226
-
-
Chebab, D.1
Johnson, J.2
Louie, E.3
Goossens, M.4
Kawasaki, E.5
Erlich, H.6
-
10
-
-
0027932851
-
Allelic ladder characterization of the short tandem repeat polymorphism located in the 5′ flanking region to the human coagulation factor A subunit gene
-
Puers C, Hammond HA, Caskey T, Lins AM, Sprecher CJ, Brinkman B, Schumm JW: Allelic ladder characterization of the short tandem repeat polymorphism located in the 5′ flanking region to the human coagulation factor A subunit gene. Genomics 1994;23:260-264
-
(1994)
Genomics
, vol.23
, pp. 260-264
-
-
Puers, C.1
Hammond, H.A.2
Caskey, T.3
Lins, A.M.4
Sprecher, C.J.5
Brinkman, B.6
Schumm, J.W.7
-
11
-
-
0026795165
-
Feasibility of prenatal diagnosis of beta-thalassemia using two highly polymorphic microsatellites 5′ to the beta-globin gene
-
Loudianos G, Cao A, Pirastu M: Feasibility of prenatal diagnosis of beta-thalassemia using two highly polymorphic microsatellites 5′ to the beta-globin gene. Haematologica 1992; 77:361-362
-
(1992)
Haematologica
, vol.77
, pp. 361-362
-
-
Loudianos, G.1
Cao, A.2
Pirastu, M.3
-
12
-
-
0031404915
-
Preimplantation diagnosis of single gene disorders by two-Step oocyte genetic analysis using first and second polar body
-
Verlinsky Y, Rechitsky S, Cieslak J, Ivakhnenko V, Wolf G, Lifchez A, Kaplan B, Moise J, Walle J, White M, Ginsberg N, Strom C, Kuliev A: Preimplantation diagnosis of single gene disorders by two-Step oocyte genetic analysis using first and second polar body. Biochem Mol Med 1997;62:182-187
-
(1997)
Biochem Mol Med
, vol.62
, pp. 182-187
-
-
Verlinsky, Y.1
Rechitsky, S.2
Cieslak, J.3
Ivakhnenko, V.4
Wolf, G.5
Lifchez, A.6
Kaplan, B.7
Moise, J.8
Walle, J.9
White, M.10
Ginsberg, N.11
Strom, C.12
Kuliev, A.13
-
13
-
-
0026849362
-
Tetra nucleotide repeat polymorphism at the D21S11 locus
-
Sharma V, Litt M: Tetra nucleotide repeat polymorphism at the D21S11 locus. Hum Mol Genet 1992;1:67
-
(1992)
Hum Mol Genet
, vol.1
, pp. 67
-
-
Sharma, V.1
Litt, M.2
-
14
-
-
0025183086
-
Family studies and prenatal diagnosis in severe Von Willebrand disease by polymerase chain reaction amplification of variable tandem repeat region of the Von Willebrand factor gene
-
Peake IR, Bowen D, Bignell P, Liddel MB, Ladler GE, Standen G, Bloom AL: Family studies and prenatal diagnosis in severe Von Willebrand disease by polymerase chain reaction amplification of variable tandem repeat region of the Von Willebrand factor gene. Blood 1990; 76:555-561
-
(1990)
Blood
, vol.76
, pp. 555-561
-
-
Peake, I.R.1
Bowen, D.2
Bignell, P.3
Liddel, M.B.4
Ladler, G.E.5
Standen, G.6
Bloom, A.L.7
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