(Q57672621)

3

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author name string

Barbara Fritz

1

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Mücevher Aslan

2

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Mette Ramsing

4

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Brigitte Fuchs

6

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Helga Rehder

European Journal of Human Genetics

7

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publication date

December 2001

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published in

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volume

9

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issue

12

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page(s)

910-916

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200741

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cites work

Mechanisms leading to uniparental disomy and their clinical consequences

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Genomic imprinting related to prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Sex ratio and absence of uniparental disomy in spontaneous abortions with a normal karyotype.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Early embryonic failure associated with uniparental disomy for human chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Trisomy 9: review and report of two new cases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Trisomy 9 syndrome: report of a case with Crohn disease and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Cytogenetic and age-dependent risk factors associated with uniparental disomy 15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Maternal uniparental disomy of chromosome 21 in a normal child

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Preimplantation genetic diagnosis: strategies and surprises

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

"Compensatory" uniparental disomy of chromosome 21 in two cases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021

Uniparental isodisomy due to duplication of chromosome 21 occuring in somatic cells monosomic for chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200741

7 January 2021