nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Author index
|
|
|
2010 |
20 |
S1 |
p. S43-S46 4 p. |
artikel |
2 |
C25 AMH in human follicular fluid
|
Dewailly, D. |
|
2010 |
20 |
S1 |
p. S7- 1 p. |
artikel |
3 |
C9 Can we build a human cell based model: SMA
|
Di Giorgio, F.P. |
|
2010 |
20 |
S1 |
p. S3- 1 p. |
artikel |
4 |
C36 Cervical washing
|
Dupont-Bernabé, C. |
|
2010 |
20 |
S1 |
p. S11- 1 p. |
artikel |
5 |
C30 Clinical relevance of male meiosis and sperm aneuploidy
|
Martin, R.H. |
|
2010 |
20 |
S1 |
p. S9- 1 p. |
artikel |
6 |
C37 Clinical validation of a non-invasive test for prenatal diagnosis of cystic fibrosis and spinal muscular atrophy based on genetic analysis of circulating trophoblastic cells
|
Paterlini-Brechot, P. |
|
2010 |
20 |
S1 |
p. S11-S12 2 p. |
artikel |
7 |
C32 Comprehensive microarray genetic analyses on single cell(s) from polar bodies or embryos to determine 23-chromosome aneuploidy, structural chromosome aberrations and genome-wide scans using single nucleotide polymorphisms (SNPs); to identify what partner provided the extra chromosome in aneuploid embryos; and to determine what embryo implanted following an in vitro fertilization (IVF) cycle
|
Kearns, W.G. |
|
2010 |
20 |
S1 |
p. S9- 1 p. |
artikel |
8 |
C31 Controlled ovarian stimulation: today and tomorrow
|
Frydman, R. |
|
2010 |
20 |
S1 |
p. S9- 1 p. |
artikel |
9 |
C16 Day 3 or Day 5 embryo biopsy: what is the best?
|
Cohen, J. |
|
2010 |
20 |
S1 |
p. S5- 1 p. |
artikel |
10 |
C17 Effect of embryo biopsy on subsequent development
|
Frydman, N. |
|
2010 |
20 |
S1 |
p. S5- 1 p. |
artikel |
11 |
C35 Effects of ovarian stimulation on endometrial gene expression profile
|
Pellicer, A. |
|
2010 |
20 |
S1 |
p. S10-S11 2 p. |
artikel |
12 |
C4 Emerging issues: Cost-effective PGD
|
Renwick, P. |
|
2010 |
20 |
S1 |
p. S2- 1 p. |
artikel |
13 |
C26 Follicular G-CSF appears as a non invasive biomarker of subsequent birth
|
Lédée, N. |
|
2010 |
20 |
S1 |
p. S8- 1 p. |
artikel |
14 |
C38 Future approach for testing of circulating fetal DNA
|
Costa, J.M. |
|
2010 |
20 |
S1 |
p. S12- 1 p. |
artikel |
15 |
C21 Genomic imprinting: about germ cells and maintenance of epigenetic information
|
Feil, R. |
|
2010 |
20 |
S1 |
p. S6- 1 p. |
artikel |
16 |
C20 Germ cells from stem cells and reprogrammed somatic cells
|
Nayernia, K. |
|
2010 |
20 |
S1 |
p. S6- 1 p. |
artikel |
17 |
C10 hESc and IPSc as models for genetic defects
|
Viville, S. |
|
2010 |
20 |
S1 |
p. S3- 1 p. |
artikel |
18 |
C23 Imaging
|
Ebner, T. |
|
2010 |
20 |
S1 |
p. S6-S7 2 p. |
artikel |
19 |
C34 Is there a particular COS for patients having genetic diseases?
|
Verpoest, W. |
|
2010 |
20 |
S1 |
p. S10- 1 p. |
artikel |
20 |
C18 Lessons from human embryo
|
Van de Velde, H. |
|
2010 |
20 |
S1 |
p. S5-S6 2 p. |
artikel |
21 |
C24 Non-invasive assessments of oocytes and embryos: Genomics of cumulus cells
|
Hamamah, S. |
|
2010 |
20 |
S1 |
p. S7- 1 p. |
artikel |
22 |
C3 Novel indications for preimplantation genetic diagnosis
|
Rechitsky, S. |
|
2010 |
20 |
S1 |
p. S1-S2 2 p. |
artikel |
23 |
C13 Oncogenetics and PND
|
Hughes, M. |
|
2010 |
20 |
S1 |
p. S4- 1 p. |
artikel |
24 |
C15 One vs two cell biopsy for PGD
|
Braude, P. |
|
2010 |
20 |
S1 |
p. S5- 1 p. |
artikel |
25 |
C43 PGD and children follow-up
|
Bonduelle, M. |
|
2010 |
20 |
S1 |
p. S13- 1 p. |
artikel |
26 |
C39 PGD and ethics: What limits should be assigned to the indications?
|
Simpson, J.L. |
|
2010 |
20 |
S1 |
p. S12- 1 p. |
artikel |
27 |
C19 PGD and PGS: which perspectives?
|
Liebaers, I. |
|
2010 |
20 |
S1 |
p. S6- 1 p. |
artikel |
28 |
C42 PGD and PND: Which and why for who?
|
Cordier, A.G. |
|
2010 |
20 |
S1 |
p. S12-S13 2 p. |
artikel |
29 |
C6 PGD and translocations
|
Pellestor, F. |
|
2010 |
20 |
S1 |
p. S2- 1 p. |
artikel |
30 |
C28 PGD for aneuploidy: CGH
|
Gianaroli, L. |
|
2010 |
20 |
S1 |
p. S8- 1 p. |
artikel |
31 |
C2 PGD for monogenic diseases: Molecular aspects
|
De Rycke, M. |
|
2010 |
20 |
S1 |
p. S1- 1 p. |
artikel |
32 |
C7 Preconception diagnosis for chromosomal abnormalities
|
Kuliev, A. |
|
2010 |
20 |
S1 |
p. S2-S3 2 p. |
artikel |
33 |
C14 Preimplantation aneuploidy testing outcome
|
Munné, S. |
|
2010 |
20 |
S1 |
p. S4-S5 2 p. |
artikel |
34 |
C8 Preimplantation genetic diagnosis and male infertility
|
Kahraman, S. |
|
2010 |
20 |
S1 |
p. S3- 1 p. |
artikel |
35 |
C12 Preimplantation genetic diagnosis for BRCA 1/2
|
SenGupta, S. |
|
2010 |
20 |
S1 |
p. S4- 1 p. |
artikel |
36 |
C41 Preimplantation genetic diagnosis: the recommendations of French Committee of Ethics
|
Le Coz, P. |
|
2010 |
20 |
S1 |
p. S12- 1 p. |
artikel |
37 |
C5 Quality control for PGD
|
Moutou, C. |
|
2010 |
20 |
S1 |
p. S2- 1 p. |
artikel |
38 |
C11 Report on prenatal diagnosis, pregnancy termination and preimplantation genetic diagnosis in inherited cancers in France
|
Stoppa-Lyonnet, D. |
|
2010 |
20 |
S1 |
p. S4- 1 p. |
artikel |
39 |
C40 Reprogenetics between science, medicine, and society: Socio-ethical reflections based on the practice of preimplantation genetic diagnosis in France
|
Bouffard, C. |
|
2010 |
20 |
S1 |
p. S12- 1 p. |
artikel |
40 |
C22 Stem cells and the IVF clinic
|
Murdoch, A. |
|
2010 |
20 |
S1 |
p. S6- 1 p. |
artikel |
41 |
C33 The management of poor responder for IVF with PGD
|
Tur-Kaspa, I. |
|
2010 |
20 |
S1 |
p. S10- 1 p. |
artikel |
42 |
C29 The origin of aneuploidy in humans: where we've been, where we're going
|
Hassold, T. |
|
2010 |
20 |
S1 |
p. S8-S9 2 p. |
artikel |
43 |
C1 Twenty years of designer babies
|
Handyside, A.H. |
|
2010 |
20 |
S1 |
p. S1- 1 p. |
artikel |
44 |
C27 What is an invasive technique or not in embryo selection?
|
Cohen, J. |
|
2010 |
20 |
S1 |
p. S8- 1 p. |
artikel |
45 |
Editorial Board
|
|
|
2010 |
20 |
S1 |
p. i- 1 p. |
artikel |
46 |
O12 Chromosome length correlates proportionally and negatively with aneuploidy and proportionally and positively with chromatid maldistribution
|
Schmutzler, A.G. |
|
2010 |
20 |
S1 |
p. S19- 1 p. |
artikel |
47 |
O16 Comparative genomic hybridisation (aCGH) to identify unbalanced products associated with specific chromosomal rearrangements
|
Thornhill, A. |
|
2010 |
20 |
S1 |
p. S20- 1 p. |
artikel |
48 |
O18 Comparison of differential gene expression profile between human embryo on day 3 and trophoblast of blastocyst on day 5: Molecular signature specific for each
|
Assou, S. |
|
2010 |
20 |
S1 |
p. S21- 1 p. |
artikel |
49 |
O15 Extended culture is a poor tool for selecting chromosomally normal embryos: Comparison of day-3 and day-5 embryos analyzed using comprehensive chromosome screening methods
|
Munné, S. |
|
2010 |
20 |
S1 |
p. S20- 1 p. |
artikel |
50 |
O4 First clinical application of karyomapping for PGD of Gaucher disease combined with 24 chromosome screening
|
Handyside, A. |
|
2010 |
20 |
S1 |
p. S16- 1 p. |
artikel |
51 |
O9 First report of hematopoietic cell transplantation for sickle cell disease from in-vitro fertilization-selected donor
|
Del Toro, G. |
|
2010 |
20 |
S1 |
p. S18- 1 p. |
artikel |
52 |
O19 Gene expression profile of apoptosis regulators of the Bcl-2 family during early embryonic development
|
Boumela, I. |
|
2010 |
20 |
S1 |
p. S21- 1 p. |
artikel |
53 |
O11 Human embryonic stem cells harboring an unbalanced reciprocal translocation t(11;22) as a valuable model for studying single gene dosage effects
|
Frumkin, T. |
|
2010 |
20 |
S1 |
p. S18- 1 p. |
artikel |
54 |
O2 Outcomes of 303 cycles on preimplantation Human Leukocyte Antigen typing with or without mutation analysis
|
Ekmekci, C.G. |
|
2010 |
20 |
S1 |
p. S15- 1 p. |
artikel |
55 |
O5 PGS by polar body biopsy – High aneuploidy rate independent of age
|
Acar-Perk, B. |
|
2010 |
20 |
S1 |
p. S16- 1 p. |
artikel |
56 |
O3 Preimplantation genetic diagnosis as a strategy to prevent a fetomaternal incompatibility for a highly immunogenic platelet antigen causing severe Fetal/Neonatal Alloimmune Thrombocytopenia (FNAIT)
|
Freixa, L. |
|
2010 |
20 |
S1 |
p. S15-S16 2 p. |
artikel |
57 |
O13 Preimplantation Genetic Diagnosis (PGD) for an apparently sporadic TSC2 mutation confirms the presence of germline mosaicism of paternal origin
|
Traversa, M. |
|
2010 |
20 |
S1 |
p. S19- 1 p. |
artikel |
58 |
O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism
|
Altarescu, G. |
|
2010 |
20 |
S1 |
p. S15- 1 p. |
artikel |
59 |
O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible
|
Renbaum, P. |
|
2010 |
20 |
S1 |
p. S17- 1 p. |
artikel |
60 |
O7 Quantitative analysis of DNA methylation at multiple imprinted genes in single human preimplantation embryos by pyrosequencing
|
Huntriss, J. |
|
2010 |
20 |
S1 |
p. S17- 1 p. |
artikel |
61 |
O6 Reanalysis of day 5 embryos following preimplantation genetic screening (PGS) for chromosomal abnormalities by fluorescence in situ hybridization on a single blastomere among different indication groups
|
Christopikou, D. |
|
2010 |
20 |
S1 |
p. S17- 1 p. |
artikel |
62 |
O10 Self correction of aneuploid embryos during hESC culture
|
Candan, Z.N. |
|
2010 |
20 |
S1 |
p. S18- 1 p. |
artikel |
63 |
O14 Trophectoderm biopsy and array CGH to detect unbalanced forms of t(9;15)(q22.2;q11.1) after failed FISH
|
Lynch, C. |
|
2010 |
20 |
S1 |
p. S19-S20 2 p. |
artikel |
64 |
O17 Whole genome profiling of early blocked embryos using customised genomic micro array
|
Benkhalifa, M. |
|
2010 |
20 |
S1 |
p. S20-S21 2 p. |
artikel |
65 |
P56 Acquisition of a trisomy 20 in the human embryonic stem cell line HD90
|
Pellestor, F. |
|
2010 |
20 |
S1 |
p. S41- 1 p. |
artikel |
66 |
P22 Aggressive ovarian stimulation may affect IVF outcome after PGD for reciprocal translocation carriers
|
Okutman-Emonts, O. |
|
2010 |
20 |
S1 |
p. S30- 1 p. |
artikel |
67 |
P38 Aneuploidy screening in single cells using microarray comparative genomic hybridization for preimplantational genetic diagnosis purposes
|
Martinez-Fresno, M. |
|
2010 |
20 |
S1 |
p. S35- 1 p. |
artikel |
68 |
P4 A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues
|
Iourov, I.Y. |
|
2010 |
20 |
S1 |
p. S24- 1 p. |
artikel |
69 |
P57 A new technique for polar body biopsy with laser tweezers and femtosecond laser zona pellucida drilling
|
Sergeev, S.A. |
|
2010 |
20 |
S1 |
p. S41-S42 2 p. |
artikel |
70 |
P9 A rapid hybridization method to detect chromosomes 15, 17, X and Y in the second hybridization round in a PGD cycle
|
Pérez, N. |
|
2010 |
20 |
S1 |
p. S25-S26 2 p. |
artikel |
71 |
P52 A rapid prenatal screening assay to simultaneously detect aneuploidies for all chromosomes from single CVS and amniocentesis samples using BACs on Beads™
|
Walker, R.K. |
|
2010 |
20 |
S1 |
p. S40- 1 p. |
artikel |
72 |
P27 Attempt to devise new, non-invasive prenatal diagnosis method based on fetal genetic material isolation from maternal blood
|
Grabowska, A. |
|
2010 |
20 |
S1 |
p. S32- 1 p. |
artikel |
73 |
P42 Can array CGH lead us to a non-invasive selection tool?
|
Cater, E. |
|
2010 |
20 |
S1 |
p. S37- 1 p. |
artikel |
74 |
P8 Case report: high polar bodies aneuploidy rate in a patient with severe ovarian hyperstimulation syndrome
|
Diblík, J. |
|
2010 |
20 |
S1 |
p. S25- 1 p. |
artikel |
75 |
P3 24 chromosome PGS: Position not quantity
|
Ioannou, D. |
|
2010 |
20 |
S1 |
p. S23-S24 2 p. |
artikel |
76 |
P39 Clinical results of array CGH for PGS
|
Munné, S. |
|
2010 |
20 |
S1 |
p. S36- 1 p. |
artikel |
77 |
P55 Comparison of obstetrical and neonatal outcomes of pregnancies obtained after preimplantation diagnosis versus intracytoplasmic injection
|
Lamazou, F. |
|
2010 |
20 |
S1 |
p. S41- 1 p. |
artikel |
78 |
P14 Complete or partial correction of aneuploidic embryos on day 3 forming hatching/hatched blastocysts on day 5
|
Altin, G. |
|
2010 |
20 |
S1 |
p. S27- 1 p. |
artikel |
79 |
P41 Comprehensive embryo analysis of AMA-related aneuploidies and mosaicism by Short-CGH
|
Rius, M. |
|
2010 |
20 |
S1 |
p. S36- 1 p. |
artikel |
80 |
P5 Correlation between preimplantation genetic screening for chromosomal aneuploidies and amount of embryos in IVF cycles
|
Kremenskoy, M. |
|
2010 |
20 |
S1 |
p. S24- 1 p. |
artikel |
81 |
P12 Efficacy of 24 chromosome FISH analysis in preimplantation embryos
|
Fernández, S. |
|
2010 |
20 |
S1 |
p. S26-S27 2 p. |
artikel |
82 |
P20 Embryo chromosome abnormalities of robertsonian translocation and the relashionship with the sex of the carrier and the size of the chromosomes involved
|
Oter, M. |
|
2010 |
20 |
S1 |
p. S29- 1 p. |
artikel |
83 |
P45 Ethical and legal aspects of surrogate pregnancy: opinion of French women on surrogate pregnancy
|
Alouini, S. |
|
2010 |
20 |
S1 |
p. S38- 1 p. |
artikel |
84 |
P58 Familial frameshift SRY mutation inherited from a mosaic father with hypospadias and cryptorchidy
|
Le Caignec, C. |
|
2010 |
20 |
S1 |
p. S42- 1 p. |
artikel |
85 |
P60 FSH-R polymorphism in severe types of OHSS
|
Macek Sr., M. |
|
2010 |
20 |
S1 |
p. S42- 1 p. |
artikel |
86 |
P51 High rate of chromosomal mosaicism in spontaneously aborted fetuses: Analysis of 715 consecutive cases with special emphasis to IVF
|
Vorsanova, S.G. |
|
2010 |
20 |
S1 |
p. S40- 1 p. |
artikel |
87 |
P43 Impact of slow-freezing-thawing on the gene expression profile of human metaphase II oocytes: transcriptomic study
|
Monzo, C. |
|
2010 |
20 |
S1 |
p. S37- 1 p. |
artikel |
88 |
P10 Molecular cytogenetic diagnosis in 591 married couples with reproductive failures: application for genetic counseling, IVF and PGD
|
Vorsanova, S.G. |
|
2010 |
20 |
S1 |
p. S26- 1 p. |
artikel |
89 |
P47 Nondisclosure PGD for late onset autosomal dominant diseases: revised ethical considerations
|
Tur-Kaspa, I. |
|
2010 |
20 |
S1 |
p. S38-S39 2 p. |
artikel |
90 |
P26 Ongoing pregnancy after PGD for cystic fibrosis and blastomere aneuploidy screening by Short-CGH
|
Daina, G. |
|
2010 |
20 |
S1 |
p. S31-S32 2 p. |
artikel |
91 |
P21 Outcomes of 252 preimplantation genetic diagnosis cycles for chromosomal rearrangements
|
Beyazyurek, C. |
|
2010 |
20 |
S1 |
p. S29-S30 2 p. |
artikel |
92 |
P34 Parthenogenetic activation of human oocytes as a model for PB-PGD
|
Paracchini, V. |
|
2010 |
20 |
S1 |
p. S34- 1 p. |
artikel |
93 |
P54 PGD activity in France: the French specificities
|
Di Costanzo, S. |
|
2010 |
20 |
S1 |
p. S40-S41 2 p. |
artikel |
94 |
P18 PGD for a woman carrier of a balanced reciprocal translocation (11;22) and a man with high expression of 16q22 fragile site
|
Martinez-Pasarell, O. |
|
2010 |
20 |
S1 |
p. S28-S29 2 p. |
artikel |
95 |
P13 PGD for gender selection: What is the percentage of embryos not available?
|
Aboujaoude, I. |
|
2010 |
20 |
S1 |
p. S27- 1 p. |
artikel |
96 |
P7 PGS program: coculture versus sequential culture system in advanced maternal age
|
Nogales, C. |
|
2010 |
20 |
S1 |
p. S25- 1 p. |
artikel |
97 |
P32 Pitfalls of preimplantation genetic diagnosis for mitochondrial DNA mutations by using polar body analysis
|
Gigarel, N. |
|
2010 |
20 |
S1 |
p. S33- 1 p. |
artikel |
98 |
P6 Polar body analysis by FISH: Evaluation of hybridisation efficiency
|
Woeck, M. |
|
2010 |
20 |
S1 |
p. S24-S25 2 p. |
artikel |
99 |
P19 Polar body based preimplantation genetic diagnosis for female translocation carriers in a public hospital in Austria
|
Maurer, M. |
|
2010 |
20 |
S1 |
p. S29- 1 p. |
artikel |
100 |
P35 Preimplantation diagnosis of monogenic diseases in GENNET
|
Putzova, M. |
|
2010 |
20 |
S1 |
p. S34- 1 p. |
artikel |
101 |
P1 Preimplantation genetic diagnosis and maternal age: the effect of embryo cohort size
|
Ercelen, N. |
|
2010 |
20 |
S1 |
p. S23- 1 p. |
artikel |
102 |
P24 Preimplantation genetic diagnosis for cystic fibrosis: The Montpellier center experience
|
Fernandez, C. |
|
2010 |
20 |
S1 |
p. S30-S31 2 p. |
artikel |
103 |
P29 Preimplantation genetic diagnosis for detection of the CAG repeat expansion in spinocerebellar ataxia type 6
|
Hung, C-C. |
|
2010 |
20 |
S1 |
p. S32-S33 2 p. |
artikel |
104 |
P23 Preimplantation genetic diagnosis for Fragile X syndrome
|
Fernandez, C. |
|
2010 |
20 |
S1 |
p. S30- 1 p. |
artikel |
105 |
P28 Preimplantation genetic diagnosis of enlarged vestibular aqueduct using GenomiPhi technology and primer extension mini-sequencing
|
Hung, C-C. |
|
2010 |
20 |
S1 |
p. S32- 1 p. |
artikel |
106 |
P30 Preimplantation genetic diagnosis of β-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes
|
Lin, S-Y. |
|
2010 |
20 |
S1 |
p. S33- 1 p. |
artikel |
107 |
P16 Preimplantation Genetic Diagnosis (PGD) cycles for translocations carriers. Results in a public hospital
|
López, O. |
|
2010 |
20 |
S1 |
p. S28- 1 p. |
artikel |
108 |
P36 Pre-implantation Genetic Haplotyping; KFSHRC experience
|
Qubbaj, W. |
|
2010 |
20 |
S1 |
p. S34-S35 2 p. |
artikel |
109 |
P44 Profile of genes differentially expressed in human cumulus cells according to oocyte nuclear maturation stages under in vivo conditions: Clinical applications
|
Ouandaogo, G. |
|
2010 |
20 |
S1 |
p. S37- 1 p. |
artikel |
110 |
Programme
|
|
|
2010 |
20 |
S1 |
p. v-ix nvt p. |
artikel |
111 |
P37 Routine use of PCR for PGD in translocation carriers: New developments to differentiate balanced carriers from non-carriers
|
Traversa, M.V. |
|
2010 |
20 |
S1 |
p. S35- 1 p. |
artikel |
112 |
P46 “Seriousness” and the regulation of preimplantation genetic diagnosis: the case of Down's syndrome
|
Krahn, T. |
|
2010 |
20 |
S1 |
p. S38- 1 p. |
artikel |
113 |
P2 Sex chromosome abnormalities in embryos from women undergoing PGS: Focus on meiotic errors involving the X-chromosome
|
Ghevaria, H. |
|
2010 |
20 |
S1 |
p. S23- 1 p. |
artikel |
114 |
P40 Short-CGH in a PGD for a reciprocal translocation: first clinical application
|
Rius, M. |
|
2010 |
20 |
S1 |
p. S36- 1 p. |
artikel |
115 |
P17 Sperm and lymphocyte aneuploidy in patients with translocations
|
Zotova, N. |
|
2010 |
20 |
S1 |
p. S28- 1 p. |
artikel |
116 |
P11 Sperm aneuploidy: When to stop counting?
|
Tempest, H.G. |
|
2010 |
20 |
S1 |
p. S26- 1 p. |
artikel |
117 |
P15 Sperm-FISH analysis revealed normal sperm cells for 14;14 homologous robertsonian translocation in a male carrier: A case report
|
Çinar, Ç. |
|
2010 |
20 |
S1 |
p. S27-S28 2 p. |
artikel |
118 |
P59 Sperm transcriptome profiling and spermatogenesis decays in normal and oligozoospermic patients
|
Montjean, D. |
|
2010 |
20 |
S1 |
p. S42- 1 p. |
artikel |
119 |
P49 Stem cell compliance on consent: rules and reality
|
Wallwork, T. |
|
2010 |
20 |
S1 |
p. S39- 1 p. |
artikel |
120 |
P31 Successful preimplantation genetic diagnosis (PGD) test for Hirschsprung disease
|
Burlet, P. |
|
2010 |
20 |
S1 |
p. S33- 1 p. |
artikel |
121 |
P25 The importance of genetic counseling of the men enrolled in ICSI program
|
Glinkina, Zh. |
|
2010 |
20 |
S1 |
p. S31- 1 p. |
artikel |
122 |
P33 The interest in preimplantation genetic diagnosis in late-onset monogenic diseases carriers
|
Krutílková, V. |
|
2010 |
20 |
S1 |
p. S34- 1 p. |
artikel |
123 |
P50 Travel to obtain reprogenetic services: Global and social trends
|
Couture, V. |
|
2010 |
20 |
S1 |
p. S39- 1 p. |
artikel |
124 |
P48 When to offer PGD for HLA typing to parents of a sick child: Suggested clinical guidelines
|
Tur-Kaspa, I. |
|
2010 |
20 |
S1 |
p. S39- 1 p. |
artikel |
125 |
P53 Widespread chromosome instability in different fetal tissues provides additional biological basis for the low success rate: implications for preimplantation genetic diagnosis
|
Yurov, Y.B. |
|
2010 |
20 |
S1 |
p. S40- 1 p. |
artikel |