Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line. (Q39517514)

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6 February 2020

title

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

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8

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Rachel Eiges

11

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Silvina Epsztejn-Litman

10

object named as

Silvina Epsztejn-Litman

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1

Gheona Altarescu

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Talia Eldar-Geva

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author name string

Paul Renbaum

2

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Baruch Brooks

4

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Irit Varshaver

5

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Mical Avitzour

6

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Ehud J Margalioth

7

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Deborah Elstein

9

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publication date

27 June 2011

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volume

31

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issue

9

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page(s)

853-860

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Successful polar body-based preimplantation genetic diagnosis for achondroplasia

6 February 2020

cites work

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Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations

21 January 2018

1 reference

Quantitative in vivo brain magnetic resonance spectroscopic monitoring of neurological involvement in mucopolysaccharidosis type II (Hunter Syndrome).

21 January 2018

1 reference

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos

21 January 2018

1 reference

Genetic manipulation of human embryonic stem cells.

21 January 2018

1 reference

Treating women under 36 years old without top-quality embryos on day 2: a prospective study comparing double embryo transfer with single blastocyst transfer

21 January 2018

1 reference

Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification

21 January 2018

1 reference

The UCSC Genome Browser Database

21 January 2018

1 reference

Hunter syndrome in an 11-year old girl on enzyme replacement therapy with idursulfase: brain magnetic resonance imaging features and evolution

21 January 2018

1 reference

Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).

21 January 2018

1 reference

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

Molecular basis of mucopolysaccharidosis type II in Portugal: identification of four novel mutations

21 January 2018

1 reference

Preimplantation genetic diagnosis with HLA matching.

21 January 2018

1 reference

Multiple mutation analysis of the cystic fibrosis gene in single cells.

21 January 2018

1 reference

Induced neuronal differentiation of human embryonic stem cells

21 January 2018

1 reference

Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)

21 January 2018

1 reference

Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body

21 January 2018

1 reference

Initial report from the Hunter Outcome Survey

21 January 2018

1 reference

Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy

21 January 2018

1 reference

Incidence of Hunter's syndrome

21 January 2018

1 reference

Vitrification of biopsied embryos at cleavage, morula and blastocyst stage

21 January 2018

1 reference

Simultaneous preimplantation genetic diagnosis for Tay–Sachs and Gaucher disease

21 January 2018

1 reference

A mother and daughter with the p.R443X mutation of mucopolysaccharidosis type II: Genotype and phenotype analysis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PD.2786

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6 February 2020

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