-
1
-
-
0035077234
-
Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis
-
White GC 2nd, Rosendaal F, Aledort LM, Lusher JM, Rothschild C, Ingerslev J. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 2001; 85: 560.
-
(2001)
Thromb Haemost
, vol.85
, pp. 560
-
-
White 2nd, G.C.1
Rosendaal, F.2
Aledort, L.M.3
Lusher, J.M.4
Rothschild, C.5
Ingerslev, J.6
-
2
-
-
62149150255
-
Haemophilia care then, now and in the future
-
Oldenburg J, Dolan G, Lemm G. Haemophilia care then, now and in the future. Haemophilia 2009; 15(Suppl 1): 2-7.
-
(2009)
Haemophilia
, vol.15
, Issue.SUPPL 1
, pp. 2-7
-
-
Oldenburg, J.1
Dolan, G.2
Lemm, G.3
-
3
-
-
33750731763
-
The obstetric and gynaecological management of women with inherited bleeding disorders - review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization
-
Lee CA, Chi C, Pavord SR et al. The obstetric and gynaecological management of women with inherited bleeding disorders - review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization. Haemophilia 2006; 12: 301-36.
-
(2006)
Haemophilia
, vol.12
, pp. 301-336
-
-
Lee, C.A.1
Chi, C.2
Pavord, S.R.3
-
4
-
-
34548405957
-
Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review
-
Mujezinovic F, Alfirevic Z. Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review. Obstet Gynecol 2007; 110: 687-94.
-
(2007)
Obstet Gynecol
, vol.110
, pp. 687-694
-
-
Mujezinovic, F.1
Alfirevic, Z.2
-
5
-
-
33646049049
-
Risk of third-trimester amniocentesis: a case-control study
-
Hodor JG, Poggi SH, Spong CY et al. Risk of third-trimester amniocentesis: a case-control study. Am J Perinatol 2006; 23: 177-80.
-
(2006)
Am J Perinatol
, vol.23
, pp. 177-180
-
-
Hodor, J.G.1
Poggi, S.H.2
Spong, C.Y.3
-
6
-
-
34748902610
-
Amniocentesis in the third trimester of pregnancy
-
O'Donoghue K, Giorgi L, Pontello V, Pasquini L, Kumar S. Amniocentesis in the third trimester of pregnancy. Prenat Diagn 2007; 27: 1000-4.
-
(2007)
Prenat Diagn
, vol.27
, pp. 1000-1004
-
-
O'Donoghue, K.1
Giorgi, L.2
Pontello, V.3
Pasquini, L.4
Kumar, S.5
-
7
-
-
61549101535
-
Sonographic fetal sex determination
-
Odeh M, Grinin V, Kais M, Ophir E, Bornstein J. Sonographic fetal sex determination. Obstet Gynecol Surv 2009; 64: 50-7.
-
(2009)
Obstet Gynecol Surv
, vol.64
, pp. 50-57
-
-
Odeh, M.1
Grinin, V.2
Kais, M.3
Ophir, E.4
Bornstein, J.5
-
8
-
-
0024338702
-
The sagittal sign. An early second trimester sonographic indicator of fetal gender
-
Emerson DS, Felker RE, Brown DL. The sagittal sign. An early second trimester sonographic indicator of fetal gender. J Ultrasound Med 1989; 8: 293-7.
-
(1989)
J Ultrasound Med
, vol.8
, pp. 293-297
-
-
Emerson, D.S.1
Felker, R.E.2
Brown, D.L.3
-
9
-
-
0032055594
-
Fetal sex determination by high resolution ultrasound in early pregnancy
-
Mielke G, Kiesel L, Backsch C, Erz W, Gonser M. Fetal sex determination by high resolution ultrasound in early pregnancy. Eur J Ultrasound 1998; 7: 109-14.
-
(1998)
Eur J Ultrasound
, vol.7
, pp. 109-114
-
-
Mielke, G.1
Kiesel, L.2
Backsch, C.3
Erz, W.4
Gonser, M.5
-
12
-
-
0033065959
-
Biometrical threshold of biparietal diameter for certain fetal sex assignment by ultrasound
-
Mazza V, Contu G, Falcinelli C et al. Biometrical threshold of biparietal diameter for certain fetal sex assignment by ultrasound. Ultrasound Obstet Gynecol 1999; 13: 308-11.
-
(1999)
Ultrasound Obstet Gynecol
, vol.13
, pp. 308-311
-
-
Mazza, V.1
Contu, G.2
Falcinelli, C.3
-
13
-
-
33745662155
-
Fetal gender assignment by first-trimester ultrasound
-
Efrat Z, Perri T, Ramati E, Tugendreich D, Meizner I. Fetal gender assignment by first-trimester ultrasound. Ultrasound Obstet Gynecol 2006; 27: 619-21.
-
(2006)
Ultrasound Obstet Gynecol
, vol.27
, pp. 619-621
-
-
Efrat, Z.1
Perri, T.2
Ramati, E.3
Tugendreich, D.4
Meizner, I.5
-
14
-
-
79958087361
-
Non-invasive prenatal determination of fetal sex: translating research into clinical practice
-
Hill M, Finning K, Martin P et al. Non-invasive prenatal determination of fetal sex: translating research into clinical practice. Clin Genet 2011; 80: 68-75.
-
(2011)
Clin Genet
, vol.80
, pp. 68-75
-
-
Hill, M.1
Finning, K.2
Martin, P.3
-
15
-
-
37749037035
-
Pregnancy in carriers of haemophilia
-
Chi C, Lee CA, Shiltagh N, Khan A, Pollard D, Kadir RA. Pregnancy in carriers of haemophilia. Haemophilia 2008; 14: 56-64.
-
(2008)
Haemophilia
, vol.14
, pp. 56-64
-
-
Chi, C.1
Lee, C.A.2
Shiltagh, N.3
Khan, A.4
Pollard, D.5
Kadir, R.A.6
-
16
-
-
33645000458
-
Non-invasive first trimester determination of fetal gender: a new approach for prenatal diagnosis of haemophilia
-
Chi C, Hyett JA, Finning KM, Lee CA, Kadir RA. Non-invasive first trimester determination of fetal gender: a new approach for prenatal diagnosis of haemophilia. BJOG 2006; 113: 239-42.
-
(2006)
BJOG
, vol.113
, pp. 239-242
-
-
Chi, C.1
Hyett, J.A.2
Finning, K.M.3
Lee, C.A.4
Kadir, R.A.5
-
17
-
-
33847239357
-
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia
-
Santacroce R, Vecchione G, Tomaiyolo M et al. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia 2006; 12: 417-22.
-
(2006)
Haemophilia
, vol.12
, pp. 417-422
-
-
Santacroce, R.1
Vecchione, G.2
Tomaiyolo, M.3
-
18
-
-
84857950472
-
Non-invasive tool for foetal sex determination in early gestational age
-
doi: 10.1111/j.1365-2516.2011.02537.x.
-
Mortarino M, Garagiola I, Lotta LA, Siboni SM, Semprini AE, Peyvandi F. Non-invasive tool for foetal sex determination in early gestational age. Haemophilia 2011; doi: 10.1111/j.1365-2516.2011.02537.x.
-
(2011)
Haemophilia
-
-
Mortarino, M.1
Garagiola, I.2
Lotta, L.A.3
Siboni, S.M.4
Semprini, A.E.5
Peyvandi, F.6
-
19
-
-
39149099757
-
Non-invasive fetal sex determination: impact on clinical practice
-
Finning KM, Chitty LS. Non-invasive fetal sex determination: impact on clinical practice. Semin Fetal Neonatal Med 2008; 13: 69-75.
-
(2008)
Semin Fetal Neonatal Med
, vol.13
, pp. 69-75
-
-
Finning, K.M.1
Chitty, L.S.2
-
20
-
-
79952230961
-
Incremental cost of non-invasive prenatal diagnosis versus invasive prenatal diagnosis of fetal sex in England
-
Hill M, Taffinder S, Chitty LS, Morris S. Incremental cost of non-invasive prenatal diagnosis versus invasive prenatal diagnosis of fetal sex in England. Prenat Diagn 2011; 31: 267-73.
-
(2011)
Prenat Diagn
, vol.31
, pp. 267-273
-
-
Hill, M.1
Taffinder, S.2
Chitty, L.S.3
Morris, S.4
-
21
-
-
20144387063
-
A framework for genetic service provision for haemophilia and other inherited bleeding disorders
-
Ludlam CA, Pasi KJ, Bolton-Maggs P et al. A framework for genetic service provision for haemophilia and other inherited bleeding disorders. Haemophilia 2005; 11: 145-63.
-
(2005)
Haemophilia
, vol.11
, pp. 145-163
-
-
Ludlam, C.A.1
Pasi, K.J.2
Bolton-Maggs, P.3
-
22
-
-
84863210569
-
-
The Haemophilia Alliance. A National Specification for Haemophilia and Related Conditions. The Haemophilia Alliance, Available at, Accessed September 6, 2011.
-
The Haemophilia Alliance. A National Specification for Haemophilia and Related Conditions. The Haemophilia Alliance, Available at, 2006. Accessed September 6, 2011.
-
(2006)
-
-
-
24
-
-
58149316091
-
The use of maternal plasma for prenatal RhD blood group genotyping
-
Finning K, Martin P, Daniels G. The use of maternal plasma for prenatal RhD blood group genotyping. Methods Mol Biol 2009; 496: 143-57.
-
(2009)
Methods Mol Biol
, vol.496
, pp. 143-157
-
-
Finning, K.1
Martin, P.2
Daniels, G.3
-
25
-
-
0030820687
-
The obstetric experience of carriers of haemophilia
-
Kadir RA, Economides DL, Braithwaite J, Goldman E, Lee CA. The obstetric experience of carriers of haemophilia. BJOG 1997; 104: 803-10.
-
(1997)
BJOG
, vol.104
, pp. 803-810
-
-
Kadir, R.A.1
Economides, D.L.2
Braithwaite, J.3
Goldman, E.4
Lee, C.A.5
-
26
-
-
0025063290
-
Carrier testing and prenatal diagnosis for hemophilia: experiences and attitudes of 549 potential and obligate carriers
-
Varekamp I, Suurmeijer TPBM, Bröcker-Vriends AHJT et al. Carrier testing and prenatal diagnosis for hemophilia: experiences and attitudes of 549 potential and obligate carriers. Am J Med Genet 1990; 37: 147-54.
-
(1990)
Am J Med Genet
, vol.37
, pp. 147-154
-
-
Varekamp, I.1
Suurmeijer, T.P.B.M.2
Bröcker-Vriends, A.H.J.T.3
-
27
-
-
34548316171
-
Attitudes towards and beliefs about genetic testing in the haemophilia community: a qualitative study
-
Thomas S, Herbert D, Street A, Barnes C, Boal J, Komesaroff P. Attitudes towards and beliefs about genetic testing in the haemophilia community: a qualitative study. Haemophilia 2007; 13: 633-41.
-
(2007)
Haemophilia
, vol.13
, pp. 633-641
-
-
Thomas, S.1
Herbert, D.2
Street, A.3
Barnes, C.4
Boal, J.5
Komesaroff, P.6
-
28
-
-
67649732906
-
Challenges of translating genetic tests into clinical and public health practice
-
Rogowski WH, Grosse SD, Khoury MJ. Challenges of translating genetic tests into clinical and public health practice. Nat Rev Genet 2009; 10: 489-95.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 489-495
-
-
Rogowski, W.H.1
Grosse, S.D.2
Khoury, M.J.3
-
29
-
-
72849151855
-
Population screening for genetic disorders in the 21st century: evidence, economics, and ethics
-
Grosse SD, Rogowski WH, Ross LF, Cornel MC, Dondorp WJ, Khoury MJ. Population screening for genetic disorders in the 21st century: evidence, economics, and ethics. Public Health Genomics 2010; 13: 106-15.
-
(2010)
Public Health Genomics
, vol.13
, pp. 106-115
-
-
Grosse, S.D.1
Rogowski, W.H.2
Ross, L.F.3
Cornel, M.C.4
Dondorp, W.J.5
Khoury, M.J.6
-
30
-
-
1342324899
-
Population genetic screening programmes: principles, techniques, practices, and policies
-
Godard B, ten Kate L, Evers-Kiebooms G, Ayme S. Population genetic screening programmes: principles, techniques, practices, and policies. Eur J Hum Genet 2003; 11(Suppl 2): S49-87.
-
(2003)
Eur J Hum Genet
, vol.11
, Issue.SUPPL 2
-
-
Godard, B.1
ten Kate, L.2
Evers-Kiebooms, G.3
Ayme, S.4
-
31
-
-
0037413486
-
Population screening in the age of genomic medicine
-
Khoury MJ, McCabe LL, McCabe ER. Population screening in the age of genomic medicine. N Engl J Med 2003; 348: 50-8.
-
(2003)
N Engl J Med
, vol.348
, pp. 50-58
-
-
Khoury, M.J.1
McCabe, L.L.2
McCabe, E.R.3
-
32
-
-
56849104642
-
Exploring informed choice in the context of prenatal testing: findings from a qualitative study
-
Potter BK, O'Reilly N, Etchegary H et al. Exploring informed choice in the context of prenatal testing: findings from a qualitative study. Health Expect 2008; 11: 355-65.
-
(2008)
Health Expect
, vol.11
, pp. 355-365
-
-
Potter, B.K.1
O'Reilly, N.2
Etchegary, H.3
-
33
-
-
70549105703
-
Will the introduction of non-invasive prenatal diagnostic testing erode informed choices? An experimental study of health care professionals
-
van den Heuvel A, Chitty L, Dormandy E et al. Will the introduction of non-invasive prenatal diagnostic testing erode informed choices? An experimental study of health care professionals. Patient Educ Couns 2009; 78: 24-8.
-
(2009)
Patient Educ Couns
, vol.78
, pp. 24-28
-
-
van den Heuvel, A.1
Chitty, L.2
Dormandy, E.3
|