Natural history of 39 patients with Achondroplasia.

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Natural history of 39 patients with Achondroplasia.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Natural history of 39 patients with Achondroplasia.

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Natural history of 39 patients with Achondroplasia.

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Natural history of 39 patients with Achondroplasia.

@en

Natural history of 39 patients with Achondroplasia.

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Natural history of 39 patients with Achondroplasia.

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Natural history of 39 patients with Achondroplasia.

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P1476

Natural history of 39 patients with Achondroplasia

@en

P2093

Chong Ae Kim

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Debora Romeo Bertola

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Guilherme Lopes Yamamoto

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Jose Ricardo Magliocco Ceroni

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Larissa de Cássia Testai

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Luiz Antonio Nunes de Oliveira

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Rachel Sayuri Honjo Kawahira

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Sofia Mizuho Miura Sugayama

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P2860

Parental age and mutation

Health supervision for children with achondroplasia.

Medical management of children with achondroplasia: evaluation of an Australasian cohort aged 0-5 years.

Constitutive activation of MKK6 in chondrocytes of transgenic mice inhibits proliferation and delays endochondral bone formation

Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome.

Achondroplasia is defined by recurrent G380R mutations of FGFR3

Mortality in achondroplasia.

FGF signaling in the developing endochondral skeleton.

Otolaryngologic manifestations of achondroplasia.

FGFs in endochondral skeletal development.

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e324

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P31

scholarly article

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10.6061/CLINICS/2018/E324

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P478

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P50

Diogo C. Soares

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2018-07-02T00:00:00Z

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29972438

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6005962

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