(Q41922790)

14 October 2017

title

Mosaic variegated aneuploidy with growth hormone deficiency and congenital heart defects (English)

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growth hormone deficiency

14 October 2017

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Andrew H Lane

1

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14 October 2017

Naghma Aijaz

2

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14 October 2017

Patricia Galvin-Parton

3

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14 October 2017

Joseph Lanman

4

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14 October 2017

Robert Mangano

5

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14 October 2017

Thomas A Wilson

6

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14 October 2017

language of work or name

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1 July 2002

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American Journal of Medical Genetics Part A

14 October 2017

published in

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14 October 2017

volume

110

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14 October 2017

issue

3

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14 October 2017

page(s)

273-277

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Mutations of mitotic checkpoint genes in human cancers

14 October 2017

cites work

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https://api.crossref.org/works/10.1002%2FAJMG.10462

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.10462

The DNA sequence of human chromosome 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

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.10462

Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD): report of a new case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

Chromosomal instability syndrome of total premature chromatid separation with mosaic variegated aneuploidy is defective in mitotic-spindle checkpoint.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

Evidence for a human mitotic mutant with pleiotropic effect

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

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.10462

Mosaic variegated trisomy (42,XY/43,XY, + variable) in a male pigtail macaque monkey.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

21 January 2018

The spindle checkpoint

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

Complications of growth hormone therapy in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

Mitotic disturbance associated with mosaic aneuploidies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10462

21 January 2018

Identifiers

DOI

10.1002/AJMG.10462

1 reference

14 October 2017

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