(Q34202205)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

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)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1

1 reference

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4 November 2019

Sandro Banfi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Brunella Franco

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

5

Christine M Disteche

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

Adriano Barra

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Jean-Pierre Truong

3

1 reference

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4 November 2019

publication date

1 June 2003

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4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

81

1 reference

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4 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

560-569

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

X-linked dominant inherited diseases with lethality in hemizygous males

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

STUDIES OF A FAMILY WITH THE ORAL-FACIAL-DIGITAL SYNDROME.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Escapees on the X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Identification and isolation of transcribed human X chromosome DNA sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Inactivation of the Zfx gene on the mouse X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Functional coherence of the human Y chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Expression and conservation of processed copies of the RBMX gene

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

Predicting coiled coils from protein sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900091-0

7 January 2021

10.1016/S0888-7543(03)00091-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12782125%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference