Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq (Q72220269)

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24 October 2019

title

Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq (English)

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24 October 2019

1

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24 October 2019

Orsetta Zuffardi

10

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24 October 2019

author name string

G Floridia

2

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24 October 2019

S Guioli

3

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24 October 2019

G Peverali

4

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24 October 2019

C Anichini

5

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24 October 2019

M Cisternino

6

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24 October 2019

R Casalone

7

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24 October 2019

C Danesino

8

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24 October 2019

M Fraccaro

9

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publication date

1 May 1993

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24 October 2019

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24 October 2019

volume

91

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24 October 2019

issue

4

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24 October 2019

page(s)

333-338

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https://scigraph.springernature.com/pub.10.1007/bf00217352

24 October 2019

exact match

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cites work

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

1 reference

12 December 2020

A pseudoautosomal gene in man

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12 December 2020

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

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12 December 2020

Functional disomies of the X chromosome influence the cell selection and hence the X inactivation pattern in females with balanced X-autosome translocations: A review of 122 cases

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12 December 2020

Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal

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12 December 2020

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.

1 reference

12 December 2020

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

12 December 2020

Isolation and characterization of a family of sequences dispersed on the human X chromosome

1 reference

12 December 2020

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

1 reference

12 December 2020

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

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

A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis

1 reference

12 December 2020

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

12 December 2020

Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region

1 reference

12 December 2020

Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq

1 reference

12 December 2020

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

12 December 2020

Nullisomy for the distal portion of Xp in a male child with a X/Y translocation

1 reference

12 December 2020

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

12 December 2020

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

1 reference

12 December 2020

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

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12 December 2020

High resolution R- and G-banding on the same preparation

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12 December 2020

Kallmann syndrome due to a translocation resulting in an X/Y fusion gene

1 reference

12 December 2020

X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.

1 reference

12 December 2020

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

12 December 2020

An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome

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/BF00217352

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24 October 2019

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