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Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
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Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice

Lisenka E. L. M. Vissers Timothy C Cox; A. Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Sarquis Jehee; Débora Romeo Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony Roscioli

PLoS Genetics San Francisco v. 7, n, 9, p. e1002278, sept. 2011

San Francisco 2011

Item não circula. Consulte sua biblioteca.(Acessar)

2
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Material Type:
Artigo 		Adicionar ao Meu Espaço

Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice

Lisenka E. L. M. Vissers Timothy C Cox; A. Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Sarquis Jehee; Débora Romeo Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony Roscioli

PLoS Genetics San Francisco v. 7, n, 9, p. e1002278, sept. 2011

San Francisco 2011

Item não circula. Consulte sua biblioteca.(Acessar)

3
A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism
A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism
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A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism

Buckley, Reuben M ; Davis, Brian W ; Brashear, Wesley A ; Farias, Fabiana H G ; Kuroki, Kei ; Graves, Tina ; Hillier, LaDeana W ; Kremitzki, Milinn ; Li, Gang ; Middleton, Rondo P ; Minx, Patrick ; Tomlinson, Chad ; Lyons, Leslie A ; Murphy, William J ; Warren, Wesley C Barsh, Gregory S.

PLoS genetics, 2020-10, Vol.16 (10), p.e1008926-e1008926 [Periódico revisado por pares]

United States: Public Library of Science

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4
A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism
A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism
Material Type:
Artigo 		Adicionar ao Meu Espaço

A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism

Buckley, Reuben M ; Davis, Brian W ; Brashear, Wesley A ; Farias, Fabiana HG ; Kuroki, Kei ; Graves, Tina ; Hillier, LaDeana W ; Kremitzki, Milinn ; Li, Gang ; Middleton, Rondo P ; Minx, Patrick ; Tomlinson, Chad ; Lyons, Leslie A ; Murphy, William J ; Warren, Wesley C

PLOS Genetics, 2020-10, Vol.16 (10)

eScholarship, University of California

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Deste Autor:

  1. Kiyozumi, D
  2. Sekiguchi, K
  3. Cox, T
  4. Wiradjaja, F
  5. Bokhoven, H

Neste Assunto:

  1. Rare Diseases
  2. Genetic Predisposition To Disease
  3. Animals
  4. Alleles
  5. Genetics

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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