Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line-Reference-Cited by-同舟云学术

Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line

Published:2011-06-27 Issue:9 Volume:31 Page:853-860
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Altarescu Gheona,Renbaum Paul,Eldar-Geva Talia,Brooks Baruch,Varshaver Irit,Avitzour Mical,Margalioth Ehud J.,Levy-Lahad Ephrat,Elstein Deborah,Epsztejn-Litman Silvina,Eiges Rachel

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.2786/fullpdf

Reference32 articles.

1. Simultaneous preimplantation genetic diagnosis (PGD) for Tay Sachs and Gaucher disease;Altarescu;Reprod Biomed Online,2007

2. Successful polar body based preimplantation genetic diagnosis (PGD) for Achondroplasia;Altarescu;Reprod Biomed Online,2008

3. Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis (PGD) in female carriers of de novo mutations;Altarescu;Hum Reprod,2009

4. Quantitative in vivo brain magnetic resonance spectroscopic monitoring of neurological involvement in mucopolysaccharidosis type II (Hunter Syndrome);Davison;J Inherit Metab Dis,2010

5. Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos;Eiges;Cell Stem Cell,2007

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