Number of blastocysts biopsied as a predictive indicator to obtain at least one normal/balanced embryo following preimplantation genetic diagnosis with single nucleotide polymorphism microarray in translocation cases

Journal of Assisted Reproduction and Genetics ◽

10.1007/s10815-016-0831-0 ◽

2016 ◽

Vol 34 (1) ◽

pp. 51-59 ◽

Author(s):

Yi-zi Wang ◽

Chen-hui Ding ◽

Jing Wang ◽

Yan-hong Zeng ◽

Wen Zhou ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Preimplantation Genetic Diagnosis ◽

Genetic Diagnosis ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

Predictive Indicator

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Identification of a Novel Single Nucleotide Polymorphism of HADHA Gene at a Referred Primer-binding Site During Pre-diagnostic Tests for Preimplantation Genetic Diagnosis

Journal of Korean Medical Science ◽

10.3346/jkms.2006.21.5.794 ◽

2006 ◽

Vol 21 (5) ◽

pp. 794 ◽

Author(s):

Hyoung Song Lee ◽

Hye Won Choi ◽

Chun Kyu Lim ◽

Mi Kyoung Koong ◽

Inn Soo Kang ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Binding Site ◽

Preimplantation Genetic Diagnosis ◽

Diagnostic Tests ◽

Genetic Diagnosis ◽

Primer Binding Site ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

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IVF Outcomes on Patients Who Underwent Preimplantation Genetic Diagnosis (PGD) for Inherited Genetic Disorders with Concurrent 24 Chromosome Aneuploidy Screening Using Single Nucleotide Polymorphism (SNP) Microarrays

Fertility and Sterility ◽

10.1016/j.fertnstert.2013.01.057 ◽

2013 ◽

Vol 99 (3) ◽

pp. S26-S27

Author(s):

D. Potter ◽

N. Wemmer ◽

K. Merrion ◽

M. Hill ◽

M. Rabinowitz

Keyword(s):

Single Nucleotide Polymorphism ◽

Preimplantation Genetic Diagnosis ◽

Genetic Disorders ◽

Genetic Diagnosis ◽

Nucleotide Polymorphism ◽

Aneuploidy Screening ◽

Single Nucleotide ◽

Ivf Outcomes ◽

Chromosome Aneuploidy ◽

Snp Microarrays

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Preimplantation genetic diagnosis (PGD) for inherited disorders using single nucleotide polymorphism (SNP) arrays: clinical outcomes from 300 cycles

Fertility and Sterility ◽

10.1016/j.fertnstert.2015.07.877 ◽

2015 ◽

Vol 104 (3) ◽

pp. e279-e280

Author(s):

S. Jaroudi ◽

R. Prates ◽

R.E. Cabey ◽

D. Goldberg-Strassler ◽

W. Chang ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Clinical Outcomes ◽

Preimplantation Genetic Diagnosis ◽

Genetic Diagnosis ◽

Nucleotide Polymorphism ◽

Inherited Disorders ◽

Single Nucleotide ◽

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Single-gene testing combined with single nucleotide polymorphism microarray preimplantation genetic diagnosis for aneuploidy: a novel approach in optimizing pregnancy outcome

Fertility and Sterility ◽

10.1016/j.fertnstert.2010.11.025 ◽

2011 ◽

Vol 95 (5) ◽

pp. 1786.e5-1786.e8 ◽

Author(s):

Paul R. Brezina ◽

Andrew Benner ◽

Svetlana Rechitsky ◽

Anver Kuliev ◽

Ekaterina Pomerantseva ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Pregnancy Outcome ◽

Preimplantation Genetic Diagnosis ◽

Single Gene ◽

Genetic Diagnosis ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

Gene Testing ◽

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Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers

Human Reproduction ◽

10.1093/humrep/det271 ◽

2013 ◽

Vol 28 (9) ◽

pp. 2581-2592 ◽

Author(s):

Y.- Q. Tan ◽

K. Tan ◽

S.- P. Zhang ◽

F. Gong ◽

D.- H. Cheng ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Clinical Outcome ◽

Preimplantation Genetic Diagnosis ◽

Genetic Diagnosis ◽

Nucleotide Polymorphism ◽

Single Nucleotide

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Comparative study of single-nucleotide polymorphism array and next generation sequencing based strategies on triploid identification in preimplantation genetic diagnosis and screen

10.18632/oncotarget.13247 ◽

2016 ◽

Vol 7 (49) ◽

pp. 81839-81848 ◽

Author(s):

Jiawei Xu ◽

Wenbin Niu ◽

Zhaofeng Peng ◽

Xiao Bao ◽

Meixiang Zhang ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Next Generation Sequencing ◽

Comparative Study ◽

Preimplantation Genetic Diagnosis ◽

Single Nucleotide Polymorphism Array ◽

Genetic Diagnosis ◽

Next Generation ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

Generation Sequencing

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A powerful tagging Single Nucleotide Polymorphism method in terms of Next-Generation Sequencing that combines Preimplantation Genetic Diagnosis, informativity testing and aneuploidy screening

10.26226/morressier.573c1513d462b80296c98b9d ◽

2016 ◽

Author(s):

Vanessa Penacho

Keyword(s):

Single Nucleotide Polymorphism ◽

Next Generation Sequencing ◽

Preimplantation Genetic Diagnosis ◽

Genetic Diagnosis ◽

Next Generation ◽

Nucleotide Polymorphism ◽

Aneuploidy Screening ◽

Single Nucleotide ◽

Generation Sequencing

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Impact of abnormal embryonic molecular karyotype determined by single nucleotide polymorphism (SNP) microarray preimplantation genetic diagnosis (PGD) on embryo development and blastocyst formation

Fertility and Sterility ◽

10.1016/j.fertnstert.2012.07.599 ◽

2012 ◽

Vol 98 (3) ◽

pp. S162 ◽

Author(s):

G. Li ◽

H. Jin ◽

Z. Xin ◽

Y. Guo ◽

Y. Su ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Embryo Development ◽

Preimplantation Genetic Diagnosis ◽

Genetic Diagnosis ◽

Blastocyst Formation ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

Snp Microarray ◽

Molecular Karyotype

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Preimplantation genetic diagnosis for achondroplasia by two haplotyping system: short tandem repeats (STRs) and single nucleotide polymorphism (SNP)

Reproductive BioMedicine Online ◽

10.1016/j.rbmo.2017.10.088 ◽

2018 ◽

Vol 36 ◽

pp. e36-e37

Author(s):

Xiaoting Shen ◽

Yanwen Xu ◽

Haitao Wu ◽

Yanhong Zeng ◽

Chenhui Ding ◽

...

Keyword(s):

Single Nucleotide Polymorphism ◽

Preimplantation Genetic Diagnosis ◽

Short Tandem Repeats ◽

Tandem Repeats ◽

Genetic Diagnosis ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

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Genetic counseling for a prenatal diagnosis of structural chromosomal abnormality with high-resolution analysis using a single nucleotide polymorphism microarray

Clinics and Practice ◽

10.4081/cp.2016.852 ◽

2016 ◽

Vol 6 (3) ◽

Author(s):

Akiko Takashima ◽

Naoki Takeshita ◽

Toshihiko Kinoshita

Keyword(s):

Single Nucleotide Polymorphism ◽

Genetic Counseling ◽

Chromosomal Abnormality ◽

Chromosomal Rearrangements ◽

Genetic Diagnosis ◽

Chromosomal Microarray ◽

Normal Male ◽

Chromosomal Microarray Analysis ◽

Nucleotide Polymorphism ◽

Single Nucleotide

A 41-year old pregnant woman underwent amniocentesis to conduct a conventional karyotyping analysis; the analysis reported an abnormal karyotype: 46,XY,add(9)(p24). Chromosomal microarray analysis (CMA) is utilized in prenatal diagnoses. A single nucleotide polymorphism microarray revealed a male fetus with balanced chromosomal translocations on 9p and balanced chromosomal rearrangements, but another chromosomal abnormality was detected. The fetus had microduplication. The child was born as a phenotypically normal male. CMA is a simple and informative procedure for prenatal genetic diagnosis. CMA is the detection of chromosomal variants of unknown clinical significance; therefore, genetic counseling is important during prenatal genetic testing.

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