-
1
-
-
0036403788
-
Prenatal diagnosis using fetal cells and cell-free fetal DNA in maternal blood: What is currently feasible?
-
HAHN, S. & W. HOLZGREVE. 2002. Prenatal diagnosis using fetal cells and cell-free fetal DNA in maternal blood: what is currently feasible? Clin. Obstet. Gynecol. 45: 649-656.
-
(2002)
Clin. Obstet. Gynecol
, vol.45
, pp. 649-656
-
-
HAHN, S.1
HOLZGREVE, W.2
-
2
-
-
0030293185
-
Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
-
CHEUNG, M.C., J.D. GOLDBERG & Y.W. KAN. 1996. Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood. Nat. Genet. 14: 264-268.
-
(1996)
Nat. Genet
, vol.14
, pp. 264-268
-
-
CHEUNG, M.C.1
GOLDBERG, J.D.2
KAN, Y.W.3
-
3
-
-
0034125028
-
Prenatal diagnosis of beta-thalassaemia using fetal erythroblasts enriched from maternal blood by a novel gradient
-
DI NARO, E., F. GHEZZI, A. VITUCCI, et al. 2000. Prenatal diagnosis of beta-thalassaemia using fetal erythroblasts enriched from maternal blood by a novel gradient. Mol. Hum. Reprod. 6: 571-574.
-
(2000)
Mol. Hum. Reprod
, vol.6
, pp. 571-574
-
-
DI NARO, E.1
GHEZZI, F.2
VITUCCI, A.3
-
5
-
-
0033968645
-
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
-
AMICUCCI, P., M. GENNARELLI, G. NOVELLI & B. DALLAPICCOLA. 2000. Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma. Clin. Chem. 46: 301-302.
-
(2000)
Clin. Chem
, vol.46
, pp. 301-302
-
-
AMICUCCI, P.1
GENNARELLI, M.2
NOVELLI, G.3
DALLAPICCOLA, B.4
-
6
-
-
0034734711
-
Prenatal DNA diagnosis of a single-gene disorder from maternal plasma
-
SAITO, H., A. SEKIZAWA, T. MORIMOTO, M. SUZUKI & T. YANAIHARA. 2000. Prenatal DNA diagnosis of a single-gene disorder from maternal plasma. Lancet 356: 1170.
-
(2000)
Lancet
, vol.356
, pp. 1170
-
-
SAITO, H.1
SEKIZAWA, A.2
MORIMOTO, T.3
SUZUKI, M.4
YANAIHARA, T.5
-
7
-
-
0036797932
-
Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma
-
GONZALEZ-GONZALEZ, M.C., M. GARCIA-HOYOS, M.J. TRUJILLO, et al. 2002. Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma. Prenat. Diagn. 22: 946-948.
-
(2002)
Prenat. Diagn
, vol.22
, pp. 946-948
-
-
GONZALEZ-GONZALEZ, M.C.1
GARCIA-HOYOS, M.2
TRUJILLO, M.J.3
-
8
-
-
0037903707
-
Prenatal detection of fetal hemoglobin E gene from maternal plasma
-
FUCHAROEN, G., W. TUNGWIWAT, T. RATANASIRI, et al. 2003. Prenatal detection of fetal hemoglobin E gene from maternal plasma. Prenat. Diagn. 23: 393-396.
-
(2003)
Prenat. Diagn
, vol.23
, pp. 393-396
-
-
FUCHAROEN, G.1
TUNGWIWAT, W.2
RATANASIRI, T.3
-
9
-
-
0037190608
-
Prenatal exclusion of beta thalassaemia major by examination of maternal plasma
-
CHIU, R.W., T.K. LAU, T.N. LEUNG, et al. 2002. Prenatal exclusion of beta thalassaemia major by examination of maternal plasma. Lancet 360: 998-1000.
-
(2002)
Lancet
, vol.360
, pp. 998-1000
-
-
CHIU, R.W.1
LAU, T.K.2
LEUNG, T.N.3
-
10
-
-
3242689524
-
Recent developments in fetal DNA in maternal plasma
-
CHIU, R.W. & Y.M. LO. 2004. Recent developments in fetal DNA in maternal plasma. Ann. N. Y. Acad. Sci. 1022: 100-104.
-
(2004)
Ann. N. Y. Acad. Sci
, vol.1022
, pp. 100-104
-
-
CHIU, R.W.1
LO, Y.M.2
-
11
-
-
1642574222
-
Size distributions of maternal and fetal DNA in maternal plasma
-
CHAN, K.C., J. ZHANG, A.B. HUI, et al. 2004. Size distributions of maternal and fetal DNA in maternal plasma. Clin. Chem. 50: 88-92.
-
(2004)
Clin. Chem
, vol.50
, pp. 88-92
-
-
CHAN, K.C.1
ZHANG, J.2
HUI, A.B.3
-
12
-
-
2642540027
-
Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms
-
LI, Y., B. ZIMMERMANN, C. RUSTERHOLZ, et al. 2004. Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms. Clin. Chem. 50: 1002-1011.
-
(2004)
Clin. Chem
, vol.50
, pp. 1002-1011
-
-
LI, Y.1
ZIMMERMANN, B.2
RUSTERHOLZ, C.3
-
13
-
-
9644273981
-
Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma - case report
-
LI, Y., W. HOLZGREVE, G.C. PAGE- CHRISTIAENS, et al. 2004. Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma - case report. Prenat. Diagn. 24: 896-898.
-
(2004)
Prenat. Diagn
, vol.24
, pp. 896-898
-
-
LI, Y.1
HOLZGREVE, W.2
PAGE- CHRISTIAENS, G.C.3
-
14
-
-
13844269123
-
Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma
-
LI, Y., E. DI NARO, A. VITUCCI, et al. 2005. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma. JAMA 293: 843-849.
-
(2005)
JAMA
, vol.293
, pp. 843-849
-
-
LI, Y.1
DI NARO, E.2
VITUCCI, A.3
-
15
-
-
2342529185
-
DNA analysis by MALDI-TOF mass spectrometry
-
GUT, I.G. 2004. DNA analysis by MALDI-TOF mass spectrometry. Hum. Mutat. 23: 437-441.
-
(2004)
Hum. Mutat
, vol.23
, pp. 437-441
-
-
GUT, I.G.1
-
16
-
-
14844303718
-
Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications
-
TOST, J. & I.G. GUT. 2005. Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications. Clin. Biochem. 38: 335-350.
-
(2005)
Clin. Biochem
, vol.38
, pp. 335-350
-
-
TOST, J.1
GUT, I.G.2
-
17
-
-
0037560709
-
Direct molecular haplotyping of long-range genomic DNA with M1-PCR
-
DING, C. & C.R. CANTOR. 2003. Direct molecular haplotyping of long-range genomic DNA with M1-PCR. Proc. Natl. Acad. Sci. USA 100: 7449-7453.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 7449-7453
-
-
DING, C.1
CANTOR, C.R.2
-
18
-
-
0347320492
-
Technology challenges in screening single gene disorders
-
BRAUN, A., R. ROTH & M.J. MCGINNISS. 2003. Technology challenges in screening single gene disorders. Eur. J. Pediatr. 162(Suppl. 1): S13-S16.
-
(2003)
Eur. J. Pediatr
, vol.162
, Issue.SUPPL. 1
-
-
BRAUN, A.1
ROTH, R.2
MCGINNISS, M.J.3
-
19
-
-
28044449568
-
Detection of trisomy 21 by quantitative mass spectrometric analysis of single-nucleotide polymorphisms
-
TSUI, N.B., R.W. CHIU, C. DING, et al. 2005. Detection of trisomy 21 by quantitative mass spectrometric analysis of single-nucleotide polymorphisms. Clin. Chem. 51: 2358-2362.
-
(2005)
Clin. Chem
, vol.51
, pp. 2358-2362
-
-
TSUI, N.B.1
CHIU, R.W.2
DING, C.3
-
20
-
-
3242703837
-
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis
-
DING, C., R.W. CHIU, T.K. LAU, et al. 2004. MS analysis of single-nucleotide differences in circulating nucleic acids: application to noninvasive prenatal diagnosis. Proc. Natl. Acad. Sci. USA 101: 10762-10767.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 10762-10767
-
-
DING, C.1
CHIU, R.W.2
LAU, T.K.3
-
21
-
-
33750267117
-
Genotyping fetal paternally inherited SNPs by MALDI-TOF MS using cell-free fetal DNA in maternal plasma: Influence of size fractionation
-
LI, Y., F. WENZEL, W. HOLZGREVE, et al. 2006. Genotyping fetal paternally inherited SNPs by MALDI-TOF MS using cell-free fetal DNA in maternal plasma: influence of size fractionation. Electrophoresis 27: 3889-3896.
-
(2006)
Electrophoresis
, vol.27
, pp. 3889-3896
-
-
LI, Y.1
WENZEL, F.2
HOLZGREVE, W.3
|