Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
 
Zoeken naar met titel:
ABCDEFGHIJKLMNOPQRSTUVWXYZ

     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             102 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Author Index 2012
 24 S2 p. S73-S76
4 p.
 artikel
2 Editorial Board 2012
 24 S2 p. i-
1 p.
 artikel
3 012 Non-invasive prenatal diagnosis of congenital adrenal hyperplasia New, M.I.
 2012
 24 S2 p. S44-
1 p.
 artikel
4 O8 Accuracy rates in biopsies performed on day-3 and day-5 embryos using CGHarray technology for PGS Mir, P.
 2012
 24 S2 p. S42-
1 p.
 artikel
5 O2 Altered morphokinetic parameters of embryos identified as aneuploid by single cell array CGH analysis at the 8-cell stage Davies, S.
 2012
 24 S2 p. S39-S40
2 p.
 artikel
6 O3 Aneuploidy screening reveals high incidence of abnormalities of chromosomes which are not involved in the rearrangements Beyazyurek, C.
 2012
 24 S2 p. S40-
1 p.
 artikel
7 O7 Assessment of 669 embryos and clinical outcome from 113 cycles using array CGH of blastomeres Veselá, K.
 2012
 24 S2 p. S42-
1 p.
 artikel
8 O11 Blastocyst trophoderm cells screening by massively parallel sequencing for aneuploidy and imbalanced chromosomal arrangements detection Yin, X.
 2012
 24 S2 p. S43-S44
2 p.
 artikel
9 O5 Determination of mutation loads in preimplantation embryos to assess the effectiveness of preimplantation genetic diagnosis (PGD) for mitochondrial DNA (mtDNA) inherited disorders Irving, L.
 2012
 24 S2 p. S41-
1 p.
 artikel
10 O6 Homozygous mutations and haplotype backgrounds; implications for PGD Renwick, P.
 2012
 24 S2 p. S41-S42
2 p.
 artikel
11 O9 Mosaicism in blastocyst stage embryos Barahona, P.
 2012
 24 S2 p. S42-S43
2 p.
 artikel
12 O1 Polar body 1, polar body 2 and blastomere analysis in PGS treatment Fishel, S.
 2012
 24 S2 p. S39-
1 p.
 artikel
13 O4 Preimplantation Genetic Diagnosis (PGD) for chromosomal rearrangements (CR) using arrays of comparative genome hybridization (aCGH). Risk assessment depending on the type of CR, the maternal age and the sex of the carrier Jimenez-Macedo, A.
 2012
 24 S2 p. S40-S41
2 p.
 artikel
14 O10 Use of next generation sequencing technology is feasible for current PGD with fresh embryo transfer Xu, K.P.
 2012
 24 S2 p. S43-
1 p.
 artikel
15 P32 Abnormal embryos showed a faster kinetic behaviour than normal embryos Nogales, M.
 2012
 24 S2 p. S58-S59
2 p.
 artikel
16 P21 Amplification refractory mutation system-quantitative polymerase chain reaction for preimplantation genetic diagnosis of β-thalassemia Chang, S.P.
 2012
 24 S2 p. S53-S54
2 p.
 artikel
17 P50 Aneuploidy testing of polar bodies by array comparative genomic hybridization (array CGH) Harasim, Th.
 2012
 24 S2 p. S67-
1 p.
 artikel
18 P48 Application of aCGH for pre-implantation genetic diagnosis of chromosome rearrangements and additional unrelated chromosome aneuploidy Lynch, C.
 2012
 24 S2 p. S66-
1 p.
 artikel
19 P56 Array-based Preimplantation Genetic Diagnosis (PGD): first experiences Heiliger, K.-J.
 2012
 24 S2 p. S69-S70
2 p.
 artikel
20 P30 Atypical cases of pre-case haplotyping analysis in GENNET Putzova, M.
 2012
 24 S2 p. S57-
1 p.
 artikel
21 P38 Birth after Preimplantation Genetic Diagnosis (PGD) using Microarray Comparative Genomic Hybridisation (MaCGH) for chromosome inversion (1) (p35q42) Lee, C.S.S.
 2012
 24 S2 p. S61-
1 p.
 artikel
22 P52 Blastocyst formation rate for aneuploid and euploid embryos in IVF cycles Feskov, O.
 2012
 24 S2 p. S68-
1 p.
 artikel
23 P28 Checking on mosaicism in day 5-blastocysts – first results from a microarray based diagnostic setting Bug, S.
 2012
 24 S2 p. S56-
1 p.
 artikel
24 P41 Chromosomal instability at different developmental stages of human preimplantation embryos Dekel-Naftali, M.
 2012
 24 S2 p. S62-S63
2 p.
 artikel
25 P54 Clinical application of array CGH on PGD/PGS with day 3 embryo biopsy Chen, C.K.
 2012
 24 S2 p. S68-S69
2 p.
 artikel
26 P6 Combination of biopsy and cryopreservation on cleavage stage human embryos Okutman-Emonts, O.
 2012
 24 S2 p. S47-
1 p.
 artikel
27 P58 Combined molecular genetic and cytogenetic analyses at the single cell level Kroneis, Th.
 2012
 24 S2 p. S70-S71
2 p.
 artikel
28 P13 Comprehensive embryo screening and the ‘best embryo’: procreative beneficence revisited Hens, K.
 2012
 24 S2 p. S50-
1 p.
 artikel
29 P46 Cytoskeletal analysis of human biopsied vs unbiopsied embryos by confocal scanning microscopy following vitrification Chatzimeletiou, K.
 2012
 24 S2 p. S65-
1 p.
 artikel
30 P40 Description of a Brazilian case of atelosteogenesis II: from prenatal to preimplantation diagnosis Sanseverino, M.T.V.
 2012
 24 S2 p. S62-
1 p.
 artikel
31 P49 Detection of chromosome copy number mosaicism in mixed cells by array comparative genome hybridization Xu, K.P.
 2012
 24 S2 p. S66-S67
2 p.
 artikel
32 P23 Detection of whole chromosome vs. chromatid errors and possible germinal mosaicism at various stages of oocyte maturation by array-CGH Ghevaria, H.
 2012
 24 S2 p. S54-
1 p.
 artikel
33 P44 Determining the parental origin of transcripts in human preimplantation embryos Tulay, P.
 2012
 24 S2 p. S64-
1 p.
 artikel
34 P29 Developmental potential of day 3 embryos diagnosed by array CGH analysis on the blastomere Cater, E.
 2012
 24 S2 p. S57-
1 p.
 artikel
35 P57 Development of a preimplantation genetic haplotyping assay for autosomal dominant retinitis pigementosa and its use for single sperm analysis to establish phase McLuskey, J.
 2012
 24 S2 p. S70-
1 p.
 artikel
36 P12 Direct counting of chromatids in polar bodies with digital PCR – a new method for aneuploidy screening in oocytes Daser, A.
 2012
 24 S2 p. S50-
1 p.
 artikel
37 P47 Effect of advanced maternal age on the stability of a preimplantation genetic screening program through one year and 347 cycles Guillén, A.
 2012
 24 S2 p. S65-S66
2 p.
 artikel
38 P11 Effects of trehalose and hyaluronic acid on motility, normal apical ridge and in vitro fertilizing ability of boar spermatozoa after cryopreservation Wang, Z.
 2012
 24 S2 p. S49-
1 p.
 artikel
39 P7 Embryo rebiopsy in PGD program – a case report Biran, G.
 2012
 24 S2 p. S47-
1 p.
 artikel
40 P14 Expression analysis of cardiometabolic genes in children born after assisted reproductive technologies De Rycke, M.
 2012
 24 S2 p. S50-S51
2 p.
 artikel
41 P20 First European report of a baby born from PGD for Vanishing White Matter disease Modamio, S.
 2012
 24 S2 p. S53-
1 p.
 artikel
42 P8 First experiences with PGD after trophectoderm biopsy at Kinderwunsch Centrum Munich (KCM), Germany Suttner, R.
 2012
 24 S2 p. S48-
1 p.
 artikel
43 P35 First Hungarian results on aneuploidy patterns of day three embryos analyzed by array comparative genome hybridization Vereczkey, A.
 2012
 24 S2 p. S60-
1 p.
 artikel
44 P27 Implementation of array-CGH technology in Preimplantation Genetic Diagnosis for rob(13;14)(q10;q10) Robertsonian translocations Xanthopoulou, L.
 2012
 24 S2 p. S56-
1 p.
 artikel
45 P19 Incorporation of non-invasive prenatal diagnosis in the management of PGD pregnancies: A new X-linked inmunodeficiency case Bustamante-Aragones, A.
 2012
 24 S2 p. S52-S53
2 p.
 artikel
46 P26 Increased pregnancy rates after trophectoderm biopsy for PGD of monogenic diseases and chromosomal aberrations Schön, U.
 2012
 24 S2 p. S55-S56
2 p.
 artikel
47 P2 Instant familial haplotyping in conjunction with embryo analysis in preimplantation genetic diagnosis (PGD) using DNA microarrays Altarescu, G.
 2012
 24 S2 p. S45-
1 p.
 artikel
48 PL6 Noninvasive prenatal diagnosis using free fetal DNA Lo, D.Y.M.
 2012
 24 S2 p. S29-
1 p.
 artikel
49 PL1 Preconception testing by next generation sequencing Kingsmore, S.
 2012
 24 S2 p. S27-
1 p.
 artikel
50 PL2 Prenatal diagnosis in the era of the personal genome Vermeesch, J.R.
 2012
 24 S2 p. S27-
1 p.
 artikel
51 PL3 Prepatterning in the mammalian embryo Zernica-Goetz, M.
 2012
 24 S2 p. S27-
1 p.
 artikel
52 PL5 The challenge of genome wide analysis in clinical practice Hengstschläger, M.
 2012
 24 S2 p. S28-
1 p.
 artikel
53 PL4 The establishment of cell lineages in the human preimplantation embryo Van de Velde, H.
 2012
 24 S2 p. S27-S28
2 p.
 artikel
54 P51 Multiple Factor PGD – 4 case reports involving testing for up to 4 indications in a single blastomere Jenner, L.
 2012
 24 S2 p. S67-
1 p.
 artikel
55 P55 Nuclear organisation in spermatozoa, a potential biomarker for male infertility? Millan, N.
 2012
 24 S2 p. S69-
1 p.
 artikel
56 P37 Oligonucleotide microarray for aneuploidies detection in single cells: implications for preimplantation genetic screening Ma, G.C.
 2012
 24 S2 p. S61-
1 p.
 artikel
57 P34 Oocyte accumulation: an efficient tool to improve preimplantation genetic diagnosis in cases of low response Parriego, M.
 2012
 24 S2 p. S59-
1 p.
 artikel
58 P59 Over-expression of ATR and XRCC1 as potential biomarkers for poor prognosis in human preimplantation embryos Bazrgar, M.
 2012
 24 S2 p. S71-
1 p.
 artikel
59 P42 PGD-AS in real indicated cases can improve the pregnancy rates Fonseca, S.A.S.
 2012
 24 S2 p. S63-
1 p.
 artikel
60 P15 PGD by FISH in India: first live-birth after PGD for a reciprocal translocation Madon, P.F.
 2012
 24 S2 p. S51-
1 p.
 artikel
61 P25 PGD in families with Robertsonian translocation of chromosomes 13 and 14 – our experience with 11 couples Peková, H.
 2012
 24 S2 p. S55-
1 p.
 artikel
62 P3 Preimplantation genetic diagnosis for BRCA2 deletion mutation using whole genome amplification and linkage analysis Chow, J.F.C.
 2012
 24 S2 p. S45-S46
2 p.
 artikel
63 P31 Preimplantation genetic diagnosis for 50 different monogenic conditions Ekmekci, C.G.
 2012
 24 S2 p. S57-S58
2 p.
 artikel
64 P33 Preimplantation genetic diagnosis for Portuguese familial amyloidotic polyneuropathy – 12 years' experience Carvalho, B.
 2012
 24 S2 p. S59-
1 p.
 artikel
65 P10 Preimplantation genetic diagnosis for the first family with Tay–Sachs disease in Cyprus Christopoulos, G.
 2012
 24 S2 p. S49-
1 p.
 artikel
66 P18 Preimplantation genetic diagnosis for translocation t(6;14)(q26;q31) using array comparative genomic hybridization at the blastocyst stage Su, Y.N.
 2012
 24 S2 p. S52-
1 p.
 artikel
67 P4 Preimplantation genetic diagnosis in four Tunisian carriers of chromosomal translocations Abdelmoula, N. Bouayed
 2012
 24 S2 p. S46-
1 p.
 artikel
68 P39 Preimplantation genetic diagnosis (PGD) for HLA matching in leukemia Yaron, Y.
 2012
 24 S2 p. S61-
1 p.
 artikel
69 P53 Recombination distribution across Major Histocompatibility Complex derived from preimplantation HLA haplotyping studies Tac, H.A.
 2012
 24 S2 p. S68-
1 p.
 artikel
70 Preimplantation Genetic Diagnosis International Society (PGDIS) 2012
 24 S2 p. iv-
1 p.
 artikel
71 P22 Restriction in cell fate of mouse embryo in the 4,5 day of development Šwitoń, K.
 2012
 24 S2 p. S54-
1 p.
 artikel
72 P45 Results from cycles with fresh and vitrified oocytes in the Preimplantation Genetic Screening program Buendía, P.
 2012
 24 S2 p. S64-
1 p.
 artikel
73 P5 Review on PGD service in Hong Kong over a decade Lee, V.C.Y.
 2012
 24 S2 p. S46-S47
2 p.
 artikel
74 P61 Risk of the ovarian hyperstimulation syndrome and FSH receptor Asn680Ser and −29A/G polymorphisms Macek Sr., M.
 2012
 24 S2 p. S71-S72
2 p.
 artikel
75 P60 The effect of longer time culture and delayed primary cell divisions on the rate of self-correction in human blastocysts Gourabi, H.
 2012
 24 S2 p. S71-
1 p.
 artikel
76 P16 The effect of maintaining Oct4 expression in the trophoblast of mouse blastocysts Donnison, M.
 2012
 24 S2 p. S51-
1 p.
 artikel
77 P1 The importance of identifying the mutation in cases of preimplantation genetic diagnosis Tomashov-Matar, R.
 2012
 24 S2 p. S45-
1 p.
 artikel
78 P36 The role of Polo-like kinase 1 in the regulation of cohesin removal during meiotic maturation of the mouse oocyte Kalleas, D.
 2012
 24 S2 p. S60-
1 p.
 artikel
79 P43 The time of internalization of inner blastomeres of mouse embryo and their later fate – is there a link? Krupa, M.
 2012
 24 S2 p. S63-S64
2 p.
 artikel
80 P17 The use of FISH and TUNEL to study the effect of GM-CSF on aneuploidy and DNA fragmentation in murine blastocysts cultured in vivo and in vitro Elaimi, A.
 2012
 24 S2 p. S51-S52
2 p.
 artikel
81 P24 Validation of preimplantation genetic screening competence and safety as a prelude to preimplantation genetic diagnosis approval in Vietnam Vu, T.B.
 2012
 24 S2 p. S55-
1 p.
 artikel
82 P9 What is the better oocytes' number in the preimplantation genetic diagnosis cycles of the male Robertsonian translocations? Huang, J.
 2012
 24 S2 p. S48-S49
2 p.
 artikel
83 S7 Blastocyst biopsy for aneuploidy screening Munné, S.
 2012
 24 S2 p. S33-S34
2 p.
 artikel
84 S14 Blastocyst biopsy for aneuploidy screening Wells, D.
 2012
 24 S2 p. S36-
1 p.
 artikel
85 S12 Chromosomal instability in the human preimplantation embryo Voet, T.
 2012
 24 S2 p. S35-
1 p.
 artikel
86 S11 Chromosomal mosaicism in the cleavage stage embryo revisited Wilton, L.
 2012
 24 S2 p. S35-
1 p.
 artikel
87 S10 Cleavage stage and blastocyst biopsy Handyside, A.H.
 2012
 24 S2 p. S35-
1 p.
 artikel
88 S19 Cost effective prevention of inherited disease by IVF and PGD Tur-Kaspa, I.
 2012
 24 S2 p. S38-
1 p.
 artikel
89 S15 EQA for new diagnostic technologies Thornhill, A.R.
 2012
 24 S2 p. S36-
1 p.
 artikel
90 S18 Four hour 24 chromosome aneuploidy screening Treff, N.
 2012
 24 S2 p. S37-
1 p.
 artikel
91 S16 Karyomapping as a means of universal diagnosis and providing insight into early human development Griffin, D.K.
 2012
 24 S2 p. S37-
1 p.
 artikel
92 S9 PGD and HLA matching: a clinical update Kahraman, S.
 2012
 24 S2 p. S34-S35
2 p.
 artikel
93 S13 PGD for aneuploidy and translocation chromosome imbalance by cleavage stage biopsy Fiorentino, F.
 2012
 24 S2 p. S36-
1 p.
 artikel
94 S8 PGD for de novo mutations (DNM) Rechitsky, S.
 2012
 24 S2 p. S34-
1 p.
 artikel
95 S6 Polar body analysis by array CGH and follow up at cleavage stages Christopikou, D.
 2012
 24 S2 p. S33-
1 p.
 artikel
96 S1 Polar body based PGD for genetic and chromosomal disorders Kuliev, A.
 2012
 24 S2 p. S31-
1 p.
 artikel
97 S3 Polar body biopsy and array CGH for aneuploidy in advanced maternal age Montag, M.
 2012
 24 S2 p. S32-
1 p.
 artikel
98 S17 The application of bioinformatics to genetic testing for the detection of human aneuploidy and genotyping Cinnioglu, C.
 2012
 24 S2 p. S37-
1 p.
 artikel
99 S4 The use of polar bodies and cumulus cells to assess oocytes and select embryos Fragouli, E.
 2012
 24 S2 p. S32-
1 p.
 artikel
100 S5 What about mitochondrial biopsy? Gianaroli, L.
 2012
 24 S2 p. S32-S33
2 p.
 artikel
101 S2 Why are human eggs so often aneuploid? A novel hypothesis from chromosome cohesion Kudo, N.R.
 2012
 24 S2 p. S31-
1 p.
 artikel
102 Welcome Handyside, Alan H.
 2012
 24 S2 p. v-
1 p.
 artikel
                             102 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland