Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy

article

Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/PD.248
P698PubMed publication ID11746168

P2093author name stringM C Magli
L Gianaroli
M Sandalinas
S Munné
T Escudero
A P Ferraretti
L Morrison
T. Escudero
L. Morrison
L. Gianaroli
M. C. Magli
A. P. Ferraretti
M. Sandalinas
S. Munné
P2860cites workComparative genomic hybridization for molecular cytogenetic analysis of solid tumorsQ29618818
Chromosome abnormalities in human embryosQ33546940
Positive outcome after preimplantation diagnosis of aneuploidy in human embryos.Q33872742
Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed.Q33880192
Outcome of preimplantation genetic diagnosis of translocationsQ33944569
Tenth anniversary of preimplantation genetic diagnosisQ34206946
Advantages of day 4 embryo transfer in patients undergoing preimplantation genetic diagnosis of aneuploidyQ36271713
Pregnancy after embryo biopsy and coamplification of DNA from X and Y chromosomesQ44844443
Mitochondrial DNA point mutation in human oocytes is associated with maternal age.Q48827069
Potential use of repeated fluorescence in situ hybridization in the same human blastomeres for preimplantation genetic diagnosisQ48930469
Influence of maternal age on meiotic spindle assembly in oocytes from naturally cycling womenQ48983154
The age-related decline in female fecundity: a quantitative controlled study of implanting capacity and survival of individual embryos after in vitro fertilization.Q49015896
Simultaneous enumeration of chromosomes 13, 18, 21, X, and Y in interphase cells for preimplantation genetic diagnosis of aneuploidy.Q50968227
Reduction in signal overlap results in increased FISH efficiency: implications for preimplantation genetic diagnosis.Q51025583
Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22Q57779445
Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysisQ57779448
Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21Q57779450
A cytogenetic study of 1000 spontaneous abortionsQ71028931
Diagnosis of major chromosome aneuploidies in human preimplantation embryosQ72347419
Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridizationQ73108832
P433issue12
P407language of work or nameEnglishQ1860
P921main subjectdiagnosisQ16644043
P304page(s)1080-5
1080-1085
P577publication date2001-12-01
P1433published inPrenatal DiagnosisQ15760059
P1476titleDouble locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy
P478volume21

Reverse relations

cites work (P2860)
Q26864151Chromosomal disorders and male infertility
Q51575238Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy.
Q53289190Does additional hybridization also improve preimplantation genetic screening results?
Q47626578ESHRE PGD Consortium 'Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)'.
Q36557326False positive rate of an arrayCGH platform for single-cell preimplantation genetic screening and subsequent clinical application on day-3
Q57005025Impact of parental gonosomal mosaicism detected in peripheral blood on preimplantation embryos
Q73832631Improved implantation after preimplantation genetic diagnosis of aneuploidy
Q57779208Improving pregnancy outcome for IVF patients with preimplantation genetic screening
Q50645612Oocyte euploidy, pronuclear zygote morphology and embryo chromosomal complement.
Q51641841Paternal contribution to aneuploidy in preimplantation embryos.
Q33601476Pre-implantation genetic screening using fluorescence in situ hybridization in couples of Indian ethnicity: Is there a scope?
Q36186429Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization.
Q73216110Preimplantation genetic diagnosis of numerical abnormalities for 13 chromosomes
Q36050002Preimplantation genetic diagnosis: the earliest form of prenatal diagnosis
Q57003418Pronuclear morphology and chromosomal abnormalities as scoring criteria for embryo selection
Q53282949The Preimplantation Genetic Diagnosis International Society (PGDIS): Guidelines for good practice in PGD.
Q50661217The beneficial effects of preimplantation genetic diagnosis for aneuploidy support extensive clinical application.
Q50651270Wide range of chromosome abnormalities in the embryos of young egg donors.

Search more.