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DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Human mutation, 2005-01, Vol.25 (1), p.56-63

2005

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548 POSTER Micronuclei in exfoliated bladder cells of gynecological cancer patients receiving pelvic radiotherapy

European journal of cancer supplements, 2007, Vol.5 (4), p.103-103

2007

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Urinary cyclophosphamide excretion and micronuclei frequencies in peripheral lymphocytes and in exfoliated buccal epithelial cells of nurses handling antineoplastics

Mutation research, 1999-02, Vol.439 (1), p.97-104

1999

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Null alleles of the aldolase B gene in patients with hereditary fructose intolerance

Journal of medical genetics, 1994-06, Vol.31 (6), p.499-503

1994

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Macrodystrophia lipomatosa of the feet and subcutaneous lipomas

American journal of medical genetics. Part A, 2003-05, Vol.119A (1), p.63-65

2003

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Chromosomal aberrations induced by radiotherapy in lymphocytes from patients with lung cancer

Journal of environmental biology, 2009-01, Vol.30 (1), p.7-10

2009

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Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter-->q22:)

Archives of gynecology and obstetrics, 2003-01, Vol.267 (3), p.173-174

2003

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Aldolase B mutations in Turkish families from central Anatolia

Genetic counseling, 2006, Vol.17 (4), p.457

2006

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DNMT3B mutations and DNA methylation defect define two types of ICF syndrome: DNMT3B AND TWO ICF SYNDROME TYPES

Human mutation, 2005-01, Vol.25 (1), p.56-63

2005

Volltextzugriff (PDF)

A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21

Clinical genetics, 2001-05, Vol.59 (5), p.368-370

2001

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46, XY gonadal dysgenesis and chronic renal failure: first reported case with Frasier syndrome from Turkey

Genetic counseling, 2004, Vol.15 (4), p.489

2004

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Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia

Genes chromosomes & cancer, 1998-01, Vol.21 (1), p.2-7

1998

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Relation between the insertion/deletion polymorphism of the angiotensin I converting enzyme gene and restenosis after coronary stenting

Journal of cardiovascular risk, 2000-12, Vol.7 (6), p.403-407

2000

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Butterfly vertebra: A case report

Clinical imaging, 2001-05, Vol.25 (3), p.206-208

2001

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A case of Prader Willi syndrome with del 15 (q11-->q13)

Turkish journal of pediatrics, 1993-10, Vol.35 (4), p.333

1993

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Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation

Clinical genetics, 1983-07, Vol.24 (1), p.47-49

1983

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A case of achondrogenesis type I

Human genetics, 1984-01, Vol.67 (3), p.349-350

1984

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Whistling face phenotype without limb abnormalities

American journal of medical genetics, 1999-09, Vol.86 (1), p.86-87

1999

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Whistling face syndrome with normal hands and feet

American journal of medical genetics, 2001-08, Vol.102 (2), p.215-215

2001

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Mental retardation with rare fragile site expressed at 2q11

Brain & development (Tokyo. 1979), 2000-12, Vol.22 (8), p.498-500

2000

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The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey

Annales de génétique, 2004-11

2004

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Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease

Journal of rheumatology, 2000-12, Vol.27 (12), p.2849

2000

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Identification of the parental origin of polysomy in two 49,XXXXY cases

Clinical genetics, 1997-06, Vol.51 (6), p.426-429

1997

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Taste sensitivity to phenylthiocarbamide in Turkey

Gene geography : a computerized bulletin on human gene frequencies, 1987-08, Vol.1 (2), p.99

1987

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Assessment of prothrombotic risk in patients with Behçet's disease should include homocysteine plasma levels

Journal of rheumatology, 2001-12, Vol.28 (12), p.2764

2001

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DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

548 POSTER Micronuclei in exfoliated bladder cells of gynecological cancer patients receiving pelvic radiotherapy

Urinary cyclophosphamide excretion and micronuclei frequencies in peripheral lymphocytes and in exfoliated buccal epithelial cells of nurses handling antineoplastics

Null alleles of the aldolase B gene in patients with hereditary fructose intolerance

Macrodystrophia lipomatosa of the feet and subcutaneous lipomas

Chromosomal aberrations induced by radiotherapy in lymphocytes from patients with lung cancer

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter-->q22:)

Aldolase B mutations in Turkish families from central Anatolia

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome: DNMT3B AND TWO ICF SYNDROME TYPES

A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21

46, XY gonadal dysgenesis and chronic renal failure: first reported case with Frasier syndrome from Turkey

Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia

Relation between the insertion/deletion polymorphism of the angiotensin I converting enzyme gene and restenosis after coronary stenting

Butterfly vertebra: A case report

A case of Prader Willi syndrome with del 15 (q11-->q13)

Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation

A case of achondrogenesis type I

Whistling face phenotype without limb abnormalities

Whistling face syndrome with normal hands and feet

Mental retardation with rare fragile site expressed at 2q11

The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease

Identification of the parental origin of polysomy in two 49,XXXXY cases

Taste sensitivity to phenylthiocarbamide in Turkey

Assessment of prothrombotic risk in patients with Behçet's disease should include homocysteine plasma levels

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