(Q33716524)

28 July 2017

1 reference

title

Sex-based differences in gene transmission and gene expression (English)

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28 July 2017

H Ostrer

1

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28 July 2017

publication date

1 January 1999

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28 July 2017

number of pages

5

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based on heuristic

inferred from page(s)

published in

Lupus

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28 July 2017

volume

8

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28 July 2017

issue

5

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28 July 2017

page(s)

365-369

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The Linkage between the Genes for Colour-Blindness and Haemophilia in Man

28 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Differential imprinting and expression of maternal and paternal genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Chromosome maps of man and mouse. IV.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Genomic imprinting determines methylation of parental alleles in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Allele-specific replication timing of imprinted gene regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Unexpected HLA haplotype sharing in dizygotic twin pairs discordant for rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Functional coherence of the human Y chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Towards the molecular localisation of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Chromosomal localisation of a Y specific growth gene(s)

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Chromosomal localisation of a gene(s) for Turner stigmata on Yp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

A human Y-chromosomal DNA sequence expressed in testicular tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

PBDX is the XG blood group gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Bibliography on X-linked mental retardation, the fragile X and related subjects IV (1988).

21 January 2018

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21 January 2018

XLMR genes: update 1992.

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https://api.crossref.org/works/10.1177%2F096120339900800507

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Primordial cell pool size and lineage relationships of five human cell types

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

X-inactivation pattern in three cases of X/autosome translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Direct Demonstration of the Mutagenic Action of Euflavine on Baker's Yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Circular Dimer and Catenate Forms of Mitochondrial DNA in Human Leukaemic Leucocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

Degree of methylation of transgenes is dependent on gamete of origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F096120339900800507

10.1177/096120339900800507

21 January 2018

Identifiers

DOI

1 reference

28 July 2017

1 reference