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Refinado por: Nome da Publicação: American Journal of Medical Genetics. Part A remover
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1
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
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Artigo 		Adicionar ao Meu Espaço

Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes

Steven B. Bleyl Janice L. B Byrne; Sarah T South; David C Dries; David A Stevenson; Alan F Rope; Angela M Vianna-Morgante; Gary C Schoenwolf; Jane D Kivlin; Arthur Brothman; John C Carey

American Journal of Medical Genetics. Part A v. 143A, n. 23, p. 2785-2795, 2007

Hoboken 2007

Item não circula. Consulte sua biblioteca.(Acessar)

2
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes

Steven B. Bleyl Janice L. B Byrne; Sarah T South; David C Dries; David A Stevenson; Alan F Rope; Angela Maria Vianna-Morgante; Gary C Schoenwolf; Jane D Kivlin; Arthur Brothman; John C Carey

American Journal of Medical Genetics. Part A v. 143A, n. 23, p. 2785-2795, 2007

Hoboken 2007

Item não circula. Consulte sua biblioteca.(Acessar)

3
Noonan syndrome in diverse populations
Noonan syndrome in diverse populations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Noonan syndrome in diverse populations

Paul Kruszka Antonio R Porras; Yonit A Addissie; Angélica Moresco; Sofia Medrano; Gary T. K Mok; Gordon K. C Leung; Cedrik Tekendo-Ngongang; Annette Uwineza; Meow-Keong Thong; Premala Muthukumarasamy; Engela Honey; Ekanem N Ekure; Ogochukwu J Sokunbi; Nnenna Kalu; Kelly L Jones; Julie D Kaplan; Omar A Abdul-Rahman; Lisa M Vincent; Amber Love; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Anju Shukla; Katta M Girisha; Siddaramappa J Patil; Nirmala D Sirisena; Vajira H. W Dissanayake; C. Sampath Paththinige; Rupesh Mishra; Eva Klein-Zighelboim; Bertha E. Gallardo Jugo; Miguel Chávez Pastor; Hugo H Abarca-Barriga; Steven A Skinner; Eloise J Prijoles; Eben Badoe; Ashleigh D Gill; Vorasuk Shotelersuk; Patroula Smpokou; Monisha S Kisling; Carlos R Ferreira; Leon Mutesa; Andre Megarbane; Antonie D Kline; Amy Kimball; Emmy Okello; Peter Lwabi; Twalib Aliku; Emmanuel Tenywa; Nonglak Boonchooduang; Pranoot Tanpaiboon; Antonio Richieri-Costa; Ambroise Wonkam; Brian H. Y Chung; Roger E Stevenson; Marshall Summar; Kausik Mandal; Shubha R Phadke; María G Obregon; Marius G Linguraru; Maximilian Muenke

American Journal of Medical Genetics. Part A Hoboken v. 173, n. 9, p. 2323-2334, Sept. 2017

Hoboken 2017

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Byrne, J
  2. Dries, D
  3. Schoenwolf, G
  4. Vianna-Morgante, A
  5. Kivlin, J

Neste Assunto:

  1. Anormalidades Cromossômicas
  2. Deleção De Genes
  3. Fenótipos
  4. Síndrome De Noonan
  5. Análise Facial

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

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