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Stegan detection method for latent images for intellectual property protection systems

Vestnik Dagestanskogo gosudarstvennogo tehničeskogo universiteta. Tehničeskie nauki (Online), 2023-02, Vol.49 (4), p.113-125

2023

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Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Cancer research (Chicago, Ill.), 2001-05, Vol.61 (10), p.4130-4135

2001

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Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

European journal of human genetics : EJHG, 1999-04, Vol.7 (3), p.287-292

1999

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Clinical and molecular studies in two families with Fraser syndrome: a new FRAS1 gene mutation, prenatal ultrasound findings and implications for genetic counselling

Genetic counseling, 2011, Vol.22 (3), p.233

2011

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Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Patients in the Black Sea Region of Turkey

Turkish journal of haematology, 2017-01, Vol.34 (4), p.345-349

2017

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Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers

Molecular human reproduction, 2006-03, Vol.12 (3), p.209-215

2006

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Acute Complete Splenic Infarction in a Patient with Hirschsprung’s Disease and Literature Review of Complete Splenic Infarction

Pathophysiology of haemostasis and thrombosis, 2008, Vol.36 (2), p.102-104

2008

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Assessment of methods online forensics in alleviation of the consequences of the attacks of extortioners

IOP conference series. Materials Science and Engineering, 2021-03, Vol.1069 (1), p.12040

2021

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Judicial technical expertise methods for investigation of cybercrimes

IOP conference series. Materials Science and Engineering, 2021-03, Vol.1069 (1), p.12041

2021

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The dependence of the performance of imaging tasks on the forensic imager interface type

IOP conference series. Materials Science and Engineering, 2021-03, Vol.1069 (1), p.12048

2021

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A new deletion of the 5α-reductase type 2 gene in a Turkish family with 5α-reductase deficiency

Clinical endocrinology (Oxford), 1995-08, Vol.43 (2), p.183-188

1995

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Using of live response technologies during the blocking of the attacks and investigation of incidents in real time

IOP conference series. Materials Science and Engineering, 2021-03, Vol.1069 (1), p.12042

2021

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The Δccr5 Mutation Conferring Protection Against HIV-1 in Caucasian Populations Has a Single and Recent Origin in Northeastern Europe

Human molecular genetics, 1998-03, Vol.7 (3), p.399-406

1998

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Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p

Genetic counseling, 2009-01, Vol.20 (4), p.341

2009

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657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family

Clinical genetics, 2002-07, Vol.62 (1), p.84-88

2002

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Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey

Journal of medical genetics, 1988-01, Vol.25 (1), p.37-40

1988

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Amyloidosis in Familial Mediterranean Fever Is Associated with a Specific Ancestral Haplotype in the MEFV Locus

Molecular genetics and metabolism, 1998-11, Vol.65 (3), p.197-202

1998

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Syndactyly, ectodermal dysplasia, and cleft lip and palate

Journal of medical genetics, 1988-07, Vol.25 (7), p.503-503

1988

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Application of the 'Apt test' in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies

Prenatal diagnosis, 1997-09, Vol.17 (9), p.879-882

1997

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Variable clinical expression of Holt-Oram syndrome in three generations

Turkish journal of pediatrics, 1998-10, Vol.40 (4), p.613

1998

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Severe intrauterine growth retardation, aged facial appearance, and congenital heart disease in a newborn with Johanson-Blizzard syndrome

Pediatric cardiology, 2000-07, Vol.21 (4), p.389-390

2000

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Impact of Fluorescence in Situ Hybridization in the Detection of Cryptic Fusion Transcript PML/RARA and A Complex t(5;15;17) in a Case of Acute Promyelocytic Leukemia

Turkish journal of haematology, 2000-12, Vol.17 (4), p.207-212

2000

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The acrocallosal syndrome in a Turkish boy

Journal of medical genetics, 1990-01, Vol.27 (1), p.48-49

1990

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Assessment of pyrin gene mutations in Turks with familial Mediterranean fever (FMF)

Human mutation, 1998, Vol.11 (6), p.456-460

1998

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Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like features

Clinical genetics, 1994-12, Vol.46 (6), p.417-422

1994

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Stegan detection method for latent images for intellectual property protection systems

Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

Clinical and molecular studies in two families with Fraser syndrome: a new FRAS1 gene mutation, prenatal ultrasound findings and implications for genetic counselling

Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Patients in the Black Sea Region of Turkey

Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers

Acute Complete Splenic Infarction in a Patient with Hirschsprung’s Disease and Literature Review of Complete Splenic Infarction

Assessment of methods online forensics in alleviation of the consequences of the attacks of extortioners

Judicial technical expertise methods for investigation of cybercrimes

The dependence of the performance of imaging tasks on the forensic imager interface type

A new deletion of the 5α-reductase type 2 gene in a Turkish family with 5α-reductase deficiency

Using of live response technologies during the blocking of the attacks and investigation of incidents in real time

The Δccr5 Mutation Conferring Protection Against HIV-1 in Caucasian Populations Has a Single and Recent Origin in Northeastern Europe

Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family

Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey

Amyloidosis in Familial Mediterranean Fever Is Associated with a Specific Ancestral Haplotype in the MEFV Locus

Syndactyly, ectodermal dysplasia, and cleft lip and palate

Application of the 'Apt test' in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies

Variable clinical expression of Holt-Oram syndrome in three generations

Severe intrauterine growth retardation, aged facial appearance, and congenital heart disease in a newborn with Johanson-Blizzard syndrome

Impact of Fluorescence in Situ Hybridization in the Detection of Cryptic Fusion Transcript PML/RARA and A Complex t(5;15;17) in a Case of Acute Promyelocytic Leukemia

The acrocallosal syndrome in a Turkish boy

Assessment of pyrin gene mutations in Turks with familial Mediterranean fever (FMF)

Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like features

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