Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

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Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

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2015年學術文章

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2015年學術文章

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Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

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Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

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Item

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Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

@en

Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

@nl

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Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

@en

Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

@nl

P1476

Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

@en

P2093

Munis Dundar

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Seda Orenay-Boyacioglu

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P2860

Latent transforming growth factor beta-binding protein 1 interacts with fibrillin and is a microfibril-associated protein

Identification and characterization of LTBP-2, a novel latent transforming growth factor-beta-binding protein

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

The latent transforming growth factor beta binding protein (LTBP) family

Role of the latent transforming growth factor beta binding protein 1 in fibrillin-containing microfibrils in bone cells in vitro and in vivo

Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3

Transforming growth factor beta 1 and its latent form binding protein-1 associate with elastic fibres in human dermis: accumulation in actinic damage and absence in anetoderma

Inactivation of Numb and Numblike in embryonic dorsal forebrain impairs neurogenesis and disrupts cortical morphogenesis

Loss of presenilin function causes impairments of memory and synaptic plasticity followed by age-dependent neurodegeneration

Targeted deletion of numb and numblike in sensory neurons reveals their essential functions in axon arborization

P304

462-467

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P31

scholarly article

P356

10.5144/0256-4947.2015.462

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P433

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P478

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Mustafa Tekin

P577

2015-11-01T00:00:00Z

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P698

26657231

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P932

6074473

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