An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis (Q81086606)

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5 January 2020

title

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

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5 January 2020

11

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5 January 2020

author name string

C Goumy

1

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5 January 2020

M Mihaescu

2

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5 January 2020

A Tchirkov

3

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5 January 2020

M Giollant

4

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5 January 2020

M N Bonnet-Dupeyron

5

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5 January 2020

J Y Jaffray

6

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5 January 2020

A Geneix

7

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5 January 2020

B Perissel

8

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5 January 2020

C Francannet

9

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5 January 2020

O Boespflug-Tanguy

10

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5 January 2020

publication date

1 June 2005

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Morphologie : bulletin de l'Association des anatomistes

5 January 2020

published in

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volume

89

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issue

285

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5 January 2020

page(s)

71-75

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Characterization of human chromosomal constitutive heterochromatin.

5 January 2020

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Structural organization of the heterochromatic region of human chromosome 9

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7 January 2021

Extra euchromatic band in the qh region of chromosome 9

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7 January 2021

Rare variant of chromosome 9

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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

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7 January 2021

Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis

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7 January 2021

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

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7 January 2021

DNA sequence and analysis of human chromosome 9

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7 January 2021

An analysis of the break points of structural rearrangements in man

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7 January 2021

Euchromatic 9q + heteromorphism in a family

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

An extra band in human 9qh+ chromosomes

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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

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7 January 2021

9qh + variant band in two families

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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

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7 January 2021

Molecular cytogenetic characterization of two types of chromosome 9 variants

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

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7 January 2021

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Identifiers

DOI

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5 January 2020

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