(Q36783772)

16 August 2017

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title

Duplication of the short arm of the X chromosome in mother and daughter (English)

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16 August 2017

C M Tuck-Muller

1

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16 August 2017

J E Martinez

2

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16 August 2017

D A Batista

3

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16 August 2017

W G Kearns

4

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16 August 2017

W Wertelecki

5

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16 August 2017

publication date

1 May 1993

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16 August 2017

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16 August 2017

volume

91

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16 August 2017

issue

4

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16 August 2017

page(s)

395-400

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Parental origin and mechanism of formation of X chromosome structural abnormalities: Four cases determined with RFLPs

16 August 2017

cites work

1 reference

12 December 2020

Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error

1 reference

12 December 2020

Inherited tandem duplication dup(X) (q131-q212) in a male proband

1 reference

12 December 2020

Clinical and cytogenetic aspects of X-chromosome deletions

1 reference

12 December 2020

Inherited partial X chromosome duplication in a mentally retarded male

1 reference

12 December 2020

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

12 December 2020

Ullrich-Turner syndrome associated with interstitial deletion of Xp11.4 leads to p22.31

1 reference

12 December 2020

X-chromosome inactivation and developmental patterns in mammals

1 reference

12 December 2020

The various phenotypes in Xp deletion. Observations in eleven patients

1 reference

12 December 2020

Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation

1 reference

12 December 2020

46, X, del (X) (p21) in a 14-year-old female with Turner signs, one streak and one normal ovary

1 reference

12 December 2020

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

1 reference

12 December 2020

A new R-banding technique in clinical cytogenetics

1 reference

12 December 2020

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

12 December 2020

Abnormality of the X chromosome in human 46,XY female siblings with dysgenetic ovaries

1 reference

12 December 2020

Probable inverted tandem duplication of Xp in a 46,Xp+Y boy

1 reference

12 December 2020

Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation

1 reference

12 December 2020

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

12 December 2020

Isolation and characterization of a major tandem repeat family from the human X chromosome

1 reference

12 December 2020

Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man

1 reference

12 December 2020

A simple technique for demonstrating centromeric heterochromatin

1 reference

12 December 2020

Partial short arm deletion of the X chromosome 46,X,del(X)(qter = to p21:)

1 reference

12 December 2020

Inherited Xq duplication due to a zygotic translocation t(X;X)(q23;q27)

1 reference

12 December 2020

A chromosomal survey of an institution for the mentally retarded. Study of 476 karyotypes with banding techniques and clinical assessment of patients with chromosome anomalies

1 reference

12 December 2020

Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BudR treatment

1 reference

12 December 2020

Partial duplication of Xp: a case report and review of previously reported cases

1 reference

12 December 2020

Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic features

1 reference

12 December 2020

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Partial short arm deletions of the X chromosome and spontaneous pubertal development in girls with short stature

1 reference

12 December 2020

Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00217366

1 reference

16 August 2017

1 reference