(Q41922387)

14 October 2017

title

Characterization of partial trisomy 9p due to insertional translocation by chromosomal (micro)FISH. (English)

1 reference

14 October 2017

1 reference

de Pater JM

1

1 reference

14 October 2017

Ippel PF

2

1 reference

14 October 2017

van Dam WM

3

1 reference

14 October 2017

Loneus WH

4

1 reference

14 October 2017

Engelen JJ

5

1 reference

14 October 2017

publication date

1 December 2002

1 reference

14 October 2017

1 reference

14 October 2017

volume

62

1 reference

14 October 2017

issue

6

1 reference

14 October 2017

page(s)

482-487

1 reference

Interchromosomal insertions. Identification of five cases and a review

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

A simple and efficient method for microdissection and microFISH.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Duplication of the short arm of chromosome 9. Analysis of five cases

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cells.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Partial duplication of the short arm of chromosome 9 (p13→p22) in a child with typical 9p trisomy phenotype

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Possible intrachromosomal duplication in a case of trisomy 9p.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Ring chromosome 9 with a 9p22.3-p24.3 duplication

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Non-syndromic mental retardation segregating with an apparently balanced t(1;17) reciprocal translocation through three generations.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

A high-resolution cytogenetic map of human chromosome 9: localization of 203 new cosmid markers by direct R-banding fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

A cell cycle regulator potentially involved in genesis of many tumor types

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

A high-resolution cytogenetic map of human chromosome 12: localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620611.X

7 January 2021

10.1034/J.1399-0004.2002.620611.X

Identifiers

DOI

1 reference

14 October 2017

1 reference