Characterization of the OFD1/Ofd1 genes on the human and mouse sex chromosomes and exclusion of Ofd1 for the Xpl mouse mutant. (Q34202205)

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4 November 2019

title

Characterization of the OFD1/Ofd1 genes on the human and mouse sex chromosomes and exclusion of Ofd1 for the Xpl mouse mutant (English)

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4 November 2019

1

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4 November 2019

Sandro Banfi

4

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4 November 2019

Brunella Franco

6

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4 November 2019

5

Christine M Disteche

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4 November 2019

author name string

Adriano Barra

2

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4 November 2019

Jean-Pierre Truong

3

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publication date

1 June 2003

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4 November 2019

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4 November 2019

volume

81

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4 November 2019

issue

6

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4 November 2019

page(s)

560-569

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X-linked dominant inherited diseases with lethality in hemizygous males

4 November 2019

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Oral-facial-digital syndrome type I: an unusual cause of hereditary cystic kidney disease

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X-linked polydactyly (Xpl), a new mutation in the mouse

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Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains

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The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.

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Identification of the gene for oral-facial-digital type I syndrome

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A first-generation X-inactivation profile of the human X chromosome

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Identification and isolation of transcribed human X chromosome DNA sequences

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Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci

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Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tarda

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A new sequence motif linking lissencephaly, Treacher Collins and oral-facial-digital type 1 syndromes, microtubule dynamics and cell migration

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Inactivation of the Zfx gene on the mouse X chromosome

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7 January 2021

A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION

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7 January 2021

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

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7 January 2021

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure

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7 January 2021

PipMaker--a web server for aligning two genomic DNA sequences

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Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse.

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Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice

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7 January 2021

Functional Coherence of the Human Y Chromosome

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Structure and organization of the RBMY genes on the human Y chromosome: transposition and amplification of an ancestral autosomal hnRNPG gene

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7 January 2021

Expression and conservation of processed copies of the RBMX gene

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7 January 2021

A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated

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7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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7 January 2021

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

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Predicting coiled coils from protein sequences

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7 January 2021

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Identifiers

DOI

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4 November 2019

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