(Q81086606)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

11

1 reference

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5 January 2020

author name string

C Goumy

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

M Mihaescu

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

A Tchirkov

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

M Giollant

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

M N Bonnet-Dupeyron

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

J Y Jaffray

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

A Geneix

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

B Perissel

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

C Francannet

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

O Boespflug-Tanguy

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

publication date

1 June 2005

1 reference

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Morphologie : bulletin de l'Association des anatomistes

5 January 2020

published in

1 reference

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5 January 2020

volume

89

1 reference

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5 January 2020

issue

285

1 reference

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5 January 2020

page(s)

71-75

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

Characterization of human chromosomal constitutive heterochromatin.

5 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect.

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Structural organization of the heterochromatic region of human chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Extra euchromatic band in the qh region of chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Rare variant of chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Characterization of double minute chromosomes' DNA content in a human high grade astrocytoma cell line by using comparative genomic hybridization and fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

DNA sequence and analysis of human chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

An analysis of the break points of structural rearrangements in man

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Euchromatic 9q + heteromorphism in a family

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

An extra band in human 9qh+ chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Identification of a break-prone structure in the 9q1 heterochromatic region

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Variants of chromosome 9 with additional euchromatic bands: two case reports

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

A half cryptic derivative der(18)t(5;18)pat identified by M-FISH and subtelomere probes: clinical findings and review of subtelomeric rearrangements

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

9qh + variant band in two families

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Investigation of the "variable spreading" of X inactivation into a translocated autosome

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

A comparison of different metaphase CGH methods for the detection of cryptic chromosome aberrations of defined size

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Two unusual G-band variants of the short arm of chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

A report of a rare chromosome 9 variant with an unusual G-banding pattern in the 9qh region.

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Size and pericentric inversion heteromorphisms of secondary constriction regions (h) of chromosomes 1, 9, and 16 as detected by CBG technique in Caucasians: Classification, frequencies, and incidence

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

Molecular cytogenetic characterization of two types of chromosome 9 variants

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents

1 reference

https://api.crossref.org/works/10.1016%2FS1286-0115%2805%2983241-2

7 January 2021

10.1016/S1286-0115(05)83241-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16110742%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference