(Q82627569)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16493556%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man (English)

1 reference

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17 January 2020

8

Patricia Jacobs

1 reference

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17 January 2020

author name string

N Simon Thomas

1

1 reference

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17 January 2020

Miranda Durkie

2

1 reference

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17 January 2020

Berendine Van Zyl

3

1 reference

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17 January 2020

Richard Sanford

4

1 reference

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17 January 2020

Gemma Potts

5

1 reference

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17 January 2020

Sheila Youings

6

1 reference

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17 January 2020

Nicholas Dennis

7

1 reference

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17 January 2020

publication date

22 February 2006

1 reference

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17 January 2020

1 reference

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17 January 2020

volume

119

1 reference

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17 January 2020

issue

4

1 reference

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17 January 2020

page(s)

444-450

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00439-006-0157-6

17 January 2020

exact match

0 references

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Molecular analysis of three patients with interstitial deletions of chromosome band 14q31

1 reference

12 December 2020

Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9

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12 December 2020

Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality

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12 December 2020

De novo proximal interstitial deletions of 14q: cytogenetic and molecular investigations

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12 December 2020

Parental origin of de novo chromosome 9 deletions in del(9p) syndrome

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12 December 2020

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

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12 December 2020

Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes

1 reference

12 December 2020

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

1 reference

12 December 2020

On the origin of chromosome anomaly

1 reference

12 December 2020

Parental origin of de novo chromosome rearrangements

1 reference

12 December 2020

Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation

1 reference

12 December 2020

Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.

1 reference

12 December 2020

Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome

1 reference

12 December 2020

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

1 reference

12 December 2020

Preferential loss of the paternal alleles in the 18q- syndrome

1 reference

12 December 2020

Turner syndrome: a cytogenetic and molecular study.

1 reference

12 December 2020