-
1
-
-
0030767241
-
Epidermolysis bullosa: A spectrum of clinical phenotypes explained by molecular heterogeneity
-
Uitto, J. et al. (1997) Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity. Mol. Med. Today 3, 457-465
-
(1997)
Mol. Med. Today
, vol.3
, pp. 457-465
-
-
Uitto, J.1
-
2
-
-
0032962217
-
Mutation analysis and molecular genetics of epidermolysis bullosa
-
Pulkkinen, L. and Uitto, J. (1999) Mutation analysis and molecular genetics of epidermolysis bullosa. Matrix Biol. 18, 29-42
-
(1999)
Matrix Biol.
, vol.18
, pp. 29-42
-
-
Pulkkinen, L.1
Uitto, J.2
-
3
-
-
0038799919
-
Prenatal diagnosis for epidermolysis bullosa: A study of 144 consecutive pregnancies at risk
-
Pfendner, E. et al. (2003) Prenatal diagnosis for epidermolysis bullosa: a study of 144 consecutive pregnancies at risk. Prenat. Diagn. 23, 447-456
-
(2003)
Prenat. Diagn.
, vol.23
, pp. 447-456
-
-
Pfendner, E.1
-
4
-
-
85031082151
-
-
Fetal Cells and DNA in the Mother Karolinum Press, Prague, Czech Republic
-
Macek, M. Sr, et al. eds (2002) Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother Karolinum Press, Prague, Czech Republic
-
(2002)
Early Prenatal Diagnosis
-
-
Macek M., Sr.1
-
5
-
-
0034864725
-
Quantification of all fetal nucleated cells in maternal blood between the 18th and 22nd weeks of pregnancy using molecular cytogenetic techniques
-
Krabchi, K. et al. (2001) Quantification of all fetal nucleated cells in maternal blood between the 18th and 22nd weeks of pregnancy using molecular cytogenetic techniques. Clin. Genet. 60, 145-150
-
(2001)
Clin. Genet.
, vol.60
, pp. 145-150
-
-
Krabchi, K.1
-
6
-
-
0030988197
-
Progress in the genetic analysis of fetal cells circulating in maternal blood
-
Bianchi, D.W. (1997) Progress in the genetic analysis of fetal cells circulating in maternal blood. Curr. Opin. Obstet. Gynecol. 9, 121-125
-
(1997)
Curr. Opin. Obstet. Gynecol.
, vol.9
, pp. 121-125
-
-
Bianchi, D.W.1
-
7
-
-
85031072631
-
The effect of the elapsed time between blood draw and processing on the recovery of fetal cells from maternal blood
-
in press
-
Sullivan, L. et al. The effect of the elapsed time between blood draw and processing on the recovery of fetal cells from maternal blood. J. Soc. Gynecol. Investig. (in press)
-
J. Soc. Gynecol. Investig.
-
-
Sullivan, L.1
-
8
-
-
0025364769
-
Isolation of fetal DNA from nucleated erythrocytes in maternal blood
-
Bianchi, D.W. et al. (1990) Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proc. Natl. Acad. Sci. U. S. A. 87, 3279-3283
-
(1990)
Proc. Natl. Acad. Sci. U. S. A.
, vol.87
, pp. 3279-3283
-
-
Bianchi, D.W.1
-
9
-
-
0027960982
-
Successful prenatal diagnosis from maternal blood with magnetic-activated cell sorting
-
Ganshirt, D. et al. (1994) Successful prenatal diagnosis from maternal blood with magnetic-activated cell sorting. Ann. N. Y. Acad. Sci. 731, 103-114
-
(1994)
Ann. N. Y. Acad. Sci.
, vol.731
, pp. 103-114
-
-
Ganshirt, D.1
-
10
-
-
85031066854
-
Cytotrophoblasts-specific antibodies for identification of fetal cells in maternal blood
-
Macek, M. Sr et al., eds, Karolinum Press, Prague, Czech Republic
-
Kilpivaara, O. et al. (2002) Cytotrophoblasts-specific antibodies for identification of fetal cells in maternal blood. In Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother (Macek, M. Sr et al., eds), pp. 34-39, Karolinum Press, Prague, Czech Republic
-
(2002)
Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother
, pp. 34-39
-
-
Kilpivaara, O.1
-
11
-
-
26344458162
-
A novel assay for rapid and simple non-invasive prenatal diagnosis of genetic anomalies
-
(Macek, M. Sr et al., eds), Karolinum Press, Prague, Czech Republic
-
Hultén, M.A. and Dhanjal, S. (2002) A novel assay for rapid and simple non-invasive prenatal diagnosis of genetic anomalies. In Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother (Macek, M. Sr et al., eds), pp. 59-71, Karolinum Press, Prague, Czech Republic
-
(2002)
Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother
, pp. 59-71
-
-
Hultén, M.A.1
Dhanjal, S.2
-
12
-
-
0026597715
-
Magnetic cell sorting and the transferrin receptor as potential means of prenatal diagnosis from maternal blood
-
Ganshirt-Ahlert, D. et al. (1992) Magnetic cell sorting and the transferrin receptor as potential means of prenatal diagnosis from maternal blood. Am. J. Obstet. Gynecol. 166, 1350-1355
-
(1992)
Am. J. Obstet. Gynecol.
, vol.166
, pp. 1350-1355
-
-
Ganshirt-Ahlert, D.1
-
13
-
-
0032748776
-
Approximately half of the erythroblasts in maternal blood are of fetal origin
-
Troeger, C. et al. (1999) Approximately half of the erythroblasts in maternal blood are of fetal origin. Mol. Hum. Reprod. 5, 1162-1165
-
(1999)
Mol. Hum. Reprod.
, vol.5
, pp. 1162-1165
-
-
Troeger, C.1
-
14
-
-
0035437180
-
Simultaneous fetal cell identification and diagnosis by ε-globin chain immunophenotyping and chromosomal fluorescence in situ hybridization
-
Choolani, M. et al. (2001) Simultaneous fetal cell identification and diagnosis by ε-globin chain immunophenotyping and chromosomal fluorescence in situ hybridization. Blood 98, 554-557
-
(2001)
Blood
, vol.98
, pp. 554-557
-
-
Choolani, M.1
-
15
-
-
0037327905
-
Circulating trophoblast in maternal blood
-
Oudejans, C.B.M. et al. (2003) Circulating trophoblast in maternal blood. Prenat. Diagn. 23, 111-116
-
(2003)
Prenat. Diagn.
, vol.23
, pp. 111-116
-
-
Oudejans, C.B.M.1
-
16
-
-
0034870468
-
Human trophoblast contains an intracellular protein reactive with an antibody against CD133 - A novel marker for trophoblast
-
Potgens, A.J. et al. (2001) Human trophoblast contains an intracellular protein reactive with an antibody against CD133 - a novel marker for trophoblast. Placenta 22, 639-645
-
(2001)
Placenta
, vol.22
, pp. 639-645
-
-
Potgens, A.J.1
-
17
-
-
0035889146
-
Identification of mesenchymal progenitor cells in human first trimester fetal blood, liver and bone marrow
-
Campagnoli, C. et al. (2001) Identification of mesenchymal progenitor cells in human first trimester fetal blood, liver and bone marrow. Blood 98, 2396-2402
-
(2001)
Blood
, vol.98
, pp. 2396-2402
-
-
Campagnoli, C.1
-
18
-
-
85031069156
-
Rediscovery of mesenchymal cells in human fetal blood
-
(Macek, M. Sr et al., eds), Karolinum Press, Prague, Czech Republic
-
Macek, M. Sr et al. (2002) Rediscovery of mesenchymal cells in human fetal blood. In Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother (Macek, M. Sr et al., eds), pp. 96-102, Karolinum Press, Prague, Czech Republic
-
(2002)
Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother
, pp. 96-102
-
-
Macek M., Sr.1
-
19
-
-
0034468279
-
Mesenchymal precursor cells in the blood of normal individuals
-
Zvaifler, N.J. et al. (2000) Mesenchymal precursor cells in the blood of normal individuals. Arthritis Res. 2, 477-488
-
(2000)
Arthritis Res.
, vol.2
, pp. 477-488
-
-
Zvaifler, N.J.1
-
20
-
-
0030893721
-
+ hematopoietic progenitor cells from maternal peripheral blood
-
+ hematopoietic progenitor cells from maternal peripheral blood. Blood 89, 2347-2358
-
(1997)
Blood
, vol.89
, pp. 2347-2358
-
-
Little, M.T.1
-
21
-
-
0033807271
-
+ progenitor cells from maternal blood samples for diagnostic purposes?
-
+ progenitor cells from maternal blood samples for diagnostic purposes? Prenat. Diagn. 20, 725-731
-
(2000)
Prenat. Diagn.
, vol.20
, pp. 725-731
-
-
Jansen, M.W.1
-
22
-
-
0030034519
-
Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum
-
Bianchi, D.W. et al. (1996) Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum. Proc. Natl. Acad. Sci. U. S. A. 93, 705-708
-
(1996)
Proc. Natl. Acad. Sci. U. S. A.
, vol.93
, pp. 705-708
-
-
Bianchi, D.W.1
-
23
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo, Y.M. et al. (1997) Presence of fetal DNA in maternal plasma and serum. Lancet 350, 485-487
-
(1997)
Lancet
, vol.350
, pp. 485-487
-
-
Lo, Y.M.1
-
24
-
-
0347898005
-
Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for non-invasive prenatal diagnosis
-
Lo, Y.M. et al. (1998) Quantitative analysis of fetal DNA in maternal plasma and serum: implications for non-invasive prenatal diagnosis. Am. J. Hum. Genet, 62, 768-775
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 768-775
-
-
Lo, Y.M.1
-
25
-
-
0033364339
-
Rapid clearance of fetal DNA from maternal plasma
-
Lo, Y.M. et al. (1999) Rapid clearance of fetal DNA from maternal plasma. Am. J. Hum. Genet. 64, 218-224
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 218-224
-
-
Lo, Y.M.1
-
26
-
-
0033762298
-
Presence of fetal RNA in maternal plasma
-
Poon, L.L. et al. (2000) Presence of fetal RNA in maternal plasma. Clin. Chem. 46, 1832-1834
-
(2000)
Clin. Chem.
, vol.46
, pp. 1832-1834
-
-
Poon, L.L.1
-
27
-
-
0037447089
-
mRNA of placental origin is readily detectable in maternal plasma
-
Ng, E.K. et al. (2003) mRNA of placental origin is readily detectable in maternal plasma. Proc. Natl. Acad. Sci. U. S. A. 100, 4748-4753
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 4748-4753
-
-
Ng, E.K.1
-
28
-
-
0032855554
-
Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy
-
Lo, Y.M. et al. (1999) Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy. Clin. Chem. 45, 1747-1751
-
(1999)
Clin. Chem.
, vol.45
, pp. 1747-1751
-
-
Lo, Y.M.1
-
29
-
-
0033751975
-
Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses
-
Zhong, X.Y. et al. (2000) Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses. Prenat. Diagn. 20, 795-798
-
(2000)
Prenat. Diagn.
, vol.20
, pp. 795-798
-
-
Zhong, X.Y.1
-
30
-
-
0032506669
-
Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
-
Lo, Y.M. et al. (1998) Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N. Engl. J. Med. 339, 1734-1738
-
(1998)
N. Engl. J. Med.
, vol.339
, pp. 1734-1738
-
-
Lo, Y.M.1
-
31
-
-
0032505654
-
Detection of fetal RHD-specific sequences in maternal plasma
-
Faas, B.H. et al. (1998) Detection of fetal RHD-specific sequences in maternal plasma. Lancet 352, 1196
-
(1998)
Lancet
, vol.352
, pp. 1196
-
-
Faas, B.H.1
-
32
-
-
0030293185
-
Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
-
Cheung, M.C. et al. (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
-
33
-
-
0036797932
-
Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma
-
Gonzales-Gonzales, M.C. 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
-
-
Gonzales-Gonzales, M.C.1
-
34
-
-
0034734711
-
Prenatal DNA diagnosis of a single-gene disorder from maternal plasma
-
Saito, H. et al. (2000) Prenatal DNA diagnosis of a single-gene disorder from maternal plasma. Lancet 356, 310-311
-
(2000)
Lancet
, vol.356
, pp. 310-311
-
-
Saito, H.1
-
35
-
-
0036231537
-
Noninvasive prenatal exclusion of congenital adrenal hyperplasia by maternal plasma analysis: A feasibility study
-
Chiu, R.W. et al. (2002) Noninvasive prenatal exclusion of congenital adrenal hyperplasia by maternal plasma analysis: a feasibility study. Clin. Chem. 48, 778-780
-
(2002)
Clin. Chem.
, vol.48
, pp. 778-780
-
-
Chiu, R.W.1
-
36
-
-
0035050166
-
Fetal DNA analyzed in plasma from a mother's three consecutive pregnancies to detect paternally inherited aneuploidy
-
Chen, C.P. et al. (2001) Fetal DNA analyzed in plasma from a mother's three consecutive pregnancies to detect paternally inherited aneuploidy. Clin. Chem. 47, 937-939
-
(2001)
Clin. Chem.
, vol.47
, pp. 937-939
-
-
Chen, C.P.1
|