(Q34587487)

3 August 2017

1 reference

title

High risk of malignancy in mosaic variegated aneuploidy syndrome. (English)

1 reference

3 August 2017

Sébastien Jacquemont

1

1 reference

3 August 2017

Michelle Bocéno

2

1 reference

3 August 2017

Jean Marie Rival

3

1 reference

3 August 2017

Françoise Méchinaud

4

1 reference

3 August 2017

Albert David

5

1 reference

3 August 2017

1 April 2002

1 reference

American Journal of Medical Genetics Part A

3 August 2017

1 reference

3 August 2017

109

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3 August 2017

1

1 reference

3 August 2017

17-21; discussion 16

1 reference

Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome.

3 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Possible new variant of Nijmegen breakage syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Variegated aneuploidy in two siblings: phenotype, genotype, CENP-E analysis, and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Mosaic variegated aneuploidy with multiple congenital abnormalities: homozygosity for total premature chromatid separation trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Evidence for a human mitotic mutant with pleiotropic effect

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Constitutional trisomy 8 and myelodysplasia: report of a case and review of the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Cytogenetic aspects of Werner's syndrome lymphocyte cultures

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

Mitotic disturbance associated with mosaic aneuploidies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

A dominantly inherited cytogenetic anomaly: a possible cell division mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10281

21 January 2018

Identifiers

DOI

10.1002/AJMG.10281

1 reference

3 August 2017

1 reference