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A New Target Radar Cross Section Based Passive Radar Surveillance Receiver Positioning Algorithm on Real Terrain Maps

Radioengineering, 2018-09, Vol.27 (3), p.891-898

Tuysuz, B.

2018

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Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity

Journal of medical genetics, 2015-08, Vol.52 (8), p.514-522

2015

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Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations

Molecular genetics and metabolism reports, 2021-06, Vol.27, p.100732-100732, Article 100732

2021

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An investigation on protection properties of Tantalum (V) oxide reinforced glass screens on unexposed breast tissue for mammography examinations

Radiography (London, England. 1995), 2024-01, Vol.30 (1), p.282-287

2024

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Development of a passive VHF radar system using software-defined radio for equatorial plasma instability studies

Radio science, 2013-07, Vol.48 (4), p.416-426

2013

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Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival

Human molecular genetics, 2009-06, Vol.18 (12), p.2149-2165

2009

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Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 cases

Clinical genetics, 2017-06, Vol.91 (6), p.868-880

2017

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Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3

Clinical genetics, 2009-04, Vol.75 (4), p.375-383

2009

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Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome

Clinical genetics, 2008-01, Vol.73 (1), p.62-70

2008

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Thyroid dysfunction in children with Down's syndrome

Acta Paediatrica, 2001-12, Vol.90 (12), p.1389-1393

2001

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Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation

Genetic counseling, 2014, Vol.25 (1), p.41

2014

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Osteoporosis-Pseudoglioma Syndrome: Three Novel Mutations in the LRP5 Gene and Response to Bisphosphonate Treatment

Hormone research in paediatrics, 2012-01, Vol.77 (2), p.115-120

2012

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Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Journal of bone and mineral research, 2016-08, Vol.31 (8), p.1577-1585

2016

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The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

Nature genetics, 2000-11, Vol.26 (3), p.370-374

2000

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Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patient

Genetic counseling, 2010-01, Vol.21 (3), p.307

2010

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Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation

Genetic counseling, 2008, Vol.19 (1), p.29

2008

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Atypical Down syndrome phenotype in a girl with 21;21 translocation trisomy

Genetic counseling, 2010, Vol.21 (1), p.61

2010

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Two novel mutations in XYLT2 cause spondyloocular syndrome

American journal of medical genetics. Part A, 2017-12, Vol.173 (12), p.3195-3200

2017

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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

Nature genetics, 2000-08, Vol.25 (4), p.419-422

2000

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CLINICAL VARIABILITY IN TWO SISTERS WITH KEUTEL SYNDROME DUE TO A HOMOZYGOUS MUTATION IN MGP GENE

Genetic counseling, 2015, Vol.26 (2), p.187

2015

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Neuroimaging and clinical characterization of Sotos syndrome

Genetic counseling, 2015, Vol.26 (1), p.1

2015

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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract

Kidney international, 2022-05, Vol.101 (5), p.1039-1053

2022

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Molecular investigations to improve diagnostic accuracy in patients with ARC syndrome

Human mutation, 2009-02, Vol.30 (2), p.E330-E337

2009

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Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

Journal of bone and mineral research, 2003-12, Vol.18 (12), p.2095-2104

2003

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A new concept of skeletal dysplasias

Turkish journal of pediatrics, 2004-07, Vol.46 (3), p.197-203

Tüysüz, Beyhan

2004

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A New Target Radar Cross Section Based Passive Radar Surveillance Receiver Positioning Algorithm on Real Terrain Maps

Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity

Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations

An investigation on protection properties of Tantalum (V) oxide reinforced glass screens on unexposed breast tissue for mammography examinations

Development of a passive VHF radar system using software-defined radio for equatorial plasma instability studies

Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival

Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 cases

Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3

Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome

Thyroid dysfunction in children with Down's syndrome

Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation

Osteoporosis-Pseudoglioma Syndrome: Three Novel Mutations in the LRP5 Gene and Response to Bisphosphonate Treatment

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patient

Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation

Atypical Down syndrome phenotype in a girl with 21;21 translocation trisomy

Two novel mutations in XYLT2 cause spondyloocular syndrome

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

CLINICAL VARIABILITY IN TWO SISTERS WITH KEUTEL SYNDROME DUE TO A HOMOZYGOUS MUTATION IN MGP GENE

Neuroimaging and clinical characterization of Sotos syndrome

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract

Molecular investigations to improve diagnostic accuracy in patients with ARC syndrome

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

A new concept of skeletal dysplasias

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