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Chromosome and sister chromatid exchange studies in Behcet's patients

Journal of dermatology, 2006-06, Vol.33 (6), p.406-410

2006

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Seckel syndrome with spontaneous chromosomal instability

Turkish journal of medical sciences, 2008-02, Vol.38 (1), p.77-81

2008

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Increased salivary level of 8-hydroxydeoxyguanosine is a marker of premature oxidative mitochondrial DNA damage in gingival tissue of patients with periodontitis

Archivum Immunologiae et Therapiae Experimentalis, 2009-06, Vol.57 (3), p.205-211

2009

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New Evidence of Premature Oxidative DNA Damage: Mitochondrial DNA Deletion in Gingival Tissue of Patients With Periodontitis

Journal of periodontology (1970), 2006-11, Vol.77 (11), p.1894-1900

2006

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Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: Report of a third family and review

American journal of medical genetics. Part A, 2009-03, Vol.149A (3), p.501-504

2009

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Molecular diagnosis of autosomal recessive non-syndromic hearing losses

Abant Medical Journal, 2012, Vol.1 (2), p.45-50

2012

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Adult height in Turkish patients with Turner syndrome without growth hormone treatment

Turkish journal of pediatrics, 2008-09, Vol.50 (5), p.415-417

2008

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Genotoxic effect of albendazole in pediatric patients with hepatic hydatid disease

International journal of infectious diseases, 2007-09, Vol.11 (5), p.446-449

2007

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Invasive lobular carcinoma of the male breast: a case report

Japanese journal of clinical oncology, 2001-09, Vol.31 (9), p.444-446

2001

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Evaluation of the genotoxic effects of chronic low-dose ionizing radiation exposure on nuclear medicine workers

Nuclear medicine and biology, 2009-07, Vol.36 (5), p.575-578

2009

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Sister Chromatid Exchange Analysis and Chromosoma Aberration Studies in Interventional Cardiology Laboratory Workers: One Year Follow up Study

Japanese Heart Journal, 2002, Vol.43(2), pp.159-166

2002

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CASE REPORT: Chromosome and sister chromatid exchange studies in Behcet's patients

Journal of dermatology, 2006-06, Vol.33 (6), p.406-410

2006

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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

Nature genetics, 1993-07, Vol.4 (3), p.289-294

1993

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A Case of Trisomy 18 Presenting with Postaxial Polydactyly and Cleft Lip and Palate

Çocuk dergisi = The journal of the pediatrics, 2013-04, Vol.12 (4), p.198-201

2013

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Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

American journal of otolaryngology, 1993-11, Vol.14 (6), p.399-403

1993

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Sister chromatid exchange analysis in patients exposed to low dose of iodine-131 for thyroid scintigraphy

Mutation research, 1997-10, Vol.393 (3), p.259-262

1997

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Sister chromatid exchange analysis and chromosoma aberration studies in interventional cardiology laboratory workers: one war follow up study

Japanese heart journal, 2002-03, Vol.43 (2), p.159

2002

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Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: Report of a third family and review

American Journal of Medical Genetics Part A, 2009, Vol.149A (3), p.501-504

2009

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Chromosome and sister chromatid exchange studies in Behcet's patients

The Journal of Dermatology, 2006, Vol.33 (6), p.406-410

2006

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Achondrogenesis type I A (Houston-harris): A case diagnosed at prenatal period

Gazi tıp dergisi, 2002, Vol.13 (3), p.149-151

2002

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Sister chromatid exchange analysis in the lymphocytes of patients with ankylosing spondylitis

Annals of the rheumatic diseases, 1997-04, Vol.56 (4), p.275-277

1997

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Comparison of sister chromatid exchange frequency between two distinct forms of anterior uveitis

Turkish journal of medical sciences, 2000, Vol.30 (1), p.71-75

2000

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Chromosome abnormalities in protein-energy malnutrition

Nutrition research (New York, N.Y.), 1996-09, Vol.16 (9), p.1487-1494

1996

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Humans
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Sister Chromatid Exchange
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Biological And Medical Sciences
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Medical Sciences
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Middle Aged
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Adolescent
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Chromosome Abnormalities
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Dna Damage
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Dna, Mitochondrial - Genetics
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Genetics & Heredity
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Aminoglycosides
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Anti-Bacterial Agents - Adverse Effects
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Chromosome and sister chromatid exchange studies in Behcet's patients

Seckel syndrome with spontaneous chromosomal instability

Increased salivary level of 8-hydroxydeoxyguanosine is a marker of premature oxidative mitochondrial DNA damage in gingival tissue of patients with periodontitis

New Evidence of Premature Oxidative DNA Damage: Mitochondrial DNA Deletion in Gingival Tissue of Patients With Periodontitis

Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: Report of a third family and review

Molecular diagnosis of autosomal recessive non-syndromic hearing losses

Adult height in Turkish patients with Turner syndrome without growth hormone treatment

Genotoxic effect of albendazole in pediatric patients with hepatic hydatid disease

Invasive lobular carcinoma of the male breast: a case report

Evaluation of the genotoxic effects of chronic low-dose ionizing radiation exposure on nuclear medicine workers

Sister Chromatid Exchange Analysis and Chromosoma Aberration Studies in Interventional Cardiology Laboratory Workers: One Year Follow up Study

CASE REPORT: Chromosome and sister chromatid exchange studies in Behcet's patients

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

A Case of Trisomy 18 Presenting with Postaxial Polydactyly and Cleft Lip and Palate

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

Sister chromatid exchange analysis in patients exposed to low dose of iodine-131 for thyroid scintigraphy

Sister chromatid exchange analysis and chromosoma aberration studies in interventional cardiology laboratory workers: one war follow up study

Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: Report of a third family and review

Chromosome and sister chromatid exchange studies in Behcet's patients

Achondrogenesis type I A (Houston-harris): A case diagnosed at prenatal period

Sister chromatid exchange analysis in the lymphocytes of patients with ankylosing spondylitis

Comparison of sister chromatid exchange frequency between two distinct forms of anterior uveitis

Chromosome abnormalities in protein-energy malnutrition

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