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Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes

Journal of neurogenetics, 2018-04, Vol.32 (2), p.65-77

2018

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Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas

Child's nervous system, 2018-05, Vol.34 (5), p.877-882

2018

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Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1

Turkish journal of pediatrics, 2011-01, Vol.53 (1), p.75-78

2011

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Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in Turkey

Child's nervous system, 2024-02, Vol.40 (2), p.511-515

2024

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Assessment of Ecotropic Viral Integration Site 2B (EVI2B) Gene in Juvenile Myelomonocytic Leukemia and Neurofibromatosis Type 1 NF1 Tumors

Biochemical genetics, 2024-04, Vol.62 (2), p.1263-1276

2024

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Coronin 1A inhibits neurite outgrowth in PC12 cells

Neuroscience letters, 2014-10, Vol.582, p.38-42

2014

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Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients

Pediatric neurology, 2007-12, Vol.37 (6), p.421-425

2007

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Familial Segmental Neurofibromatosis

Journal of child neurology, 2004-05, Vol.19 (5), p.392-394

2004

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Clinical findings and mutation analysis of NF1 patients in Turkey

Meta Gene, 2018-02, Vol.15, p.80-83

2018

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Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers

Turkish journal of pediatrics, 2003-07, Vol.45 (3), p.192-197

2003

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Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype

Child's nervous system, 2012-06, Vol.28 (6), p.943-946

2012

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Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case

BMJ case reports, 2013-02, Vol.2013, p.bcr2012008468

2013

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NF1 Gene Mutations are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome

Journal of Neurology & Stroke, 2017-05, Vol.6 (6)

Ayter, Şükriye

2017

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Neurofibromatosis—Noonan's Syndrome With Associated Rhabdomyosarcoma of the Urinary Bladder in an Infant: Case Report

Journal of child neurology, 2003-01, Vol.18 (1), p.68-72

2003

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Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype

Child's nervous system, 2011-12, Vol.27 (12), p.2113-2116

2011

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Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling

Genetic counseling, 2009-01, Vol.20 (2), p.195

2009

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Gene symbol: NF1. Disease: neurofibromatosis 1

Human genetics, 2006-04, Vol.119 (3), p.360-360

2006

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Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case

BMJ Case Reports, 2013, Vol.2013

2013

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Molecular genetic analyses in neurofibromatosis type 1 patients with tumors

Cancer genetics and cytogenetics, 2006-03, Vol.165 (2), p.167-171

2006

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Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene

Cancer genetics and cytogenetics, 2006-01, Vol.164 (2), p.159-163

2006

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Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes

Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas

Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1

Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in Turkey

Assessment of Ecotropic Viral Integration Site 2B (EVI2B) Gene in Juvenile Myelomonocytic Leukemia and Neurofibromatosis Type 1 NF1 Tumors

Coronin 1A inhibits neurite outgrowth in PC12 cells

Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients

Familial Segmental Neurofibromatosis

Clinical findings and mutation analysis of NF1 patients in Turkey

Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers

Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype

Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case

NF1 Gene Mutations are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome

Neurofibromatosis—Noonan's Syndrome With Associated Rhabdomyosarcoma of the Urinary Bladder in an Infant: Case Report

Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype

Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling

Gene symbol: NF1. Disease: neurofibromatosis 1

Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case

Molecular genetic analyses in neurofibromatosis type 1 patients with tumors

Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene

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