(Q28251879)

1

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C Lanctôt

2

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J J Tremblay

3

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N Jenkins

4

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D Gilbert

5

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N Copeland

6

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B Beatty

7

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J Drouin

Development and applications of a molecular genetic linkage map of the mouse genome

8

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language of work or name

English

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publication date

1997

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published in

Mammalian Genome

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volume

8

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issue

11

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page(s)

841-5

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cites work

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

BERRY-TREACHER COLLINS SYNDROME: A REVIEW OF 200 CASES (MANDIBULO-FACIAL DYSOSTOSIS; FRANCESCHETTI-ZWAHLEN-KLEIN SYNDROMES).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

DNA sequencing with chain-terminating inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

The expanding world of trinucleotide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Mild mandibulofacial dysostosis in a child with a deletion of 3p

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Mapping of Murine Fibroblast Growth Factor Receptors Refines Regions of Homology between Mouse and Human Chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Rapid physical mapping of cloned DNA on banded mouse chromosomes by fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Mandibulo-facial dysostosis. (Treacher-Collins syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

Modes of DAPI banding and simultaneous in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900589

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020

Treacher Collins syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020

Mandibulo-facial dysostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020

Otlx2, an Otx-related homeobox gene expressed in the pituitary gland and in a restricted pattern in the forebrain

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020

A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020

Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020

Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9337397

12 December 2020