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10 Years' Experience in Fragile X Testing Among Mentally Retarded Individuals in Greece: A Molecular and Epidemiological Approach

In vivo (Athens), 2008-07, Vol.22 (4), p.451-455

2008

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Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-ε Antibody

Fetal diagnosis and therapy, 2003-09, Vol.18 (5), p.309-313

2003

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Cohen syndrome : two new cases in siblings

European journal of pediatrics, 1999-10, Vol.158 (10), p.838-841

1999

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Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings

Clinical and laboratory haematology, 2002-12, Vol.24 (6), p.361-367

2002

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Identification of three polymorphisms in the dystrophin gene

Molecular and cellular probes, 1999-12, Vol.13 (6), p.453-454

1999

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Prenatal Diagnosis Services in Greece

European journal of human genetics : EJHG, 1997-01, Vol.5 (Suppl 1), p.39-41

1997

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Chromosome fragility and predisposition to childhood malignancies

Anticancer research, 1998-07, Vol.18 (4A), p.2359

1998

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Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol

Molecular and cellular probes, 2005-12, Vol.19 (6), p.422-424

2005

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De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia

European journal of pediatrics, 2003-09, Vol.162 (9), p.594-597

2003

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Analysis of DNA Haplotypes Suggests a Genetic Predisposition to Trisomy 21 Associated with DNA Sequences on Chromosome 21

Proceedings of the National Academy of Sciences - PNAS, 1985-05, Vol.82 (10), p.3360-3364

1985

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Detection of Fetal NRBCs in Maternal Blood of Pregnant Carriers of β-Thalassemia Using Anti-γ and Anti-ε Monoclonal Antibodies

Annals of the New York Academy of Sciences, 2001-09, Vol.945 (1), p.151-152

2001

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A 10-YEAR EXPERIENCE OF MOLECULAR TESTING IN DMD/BMD MUSCULAR DYSTROPHIES IN GREECE

Neuropediatrics, 2006, Vol.37 (S 1)

2006

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The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphisms

American journal of human genetics, 1992-03, Vol.50 (3), p.544-550

1992

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Awareness and use of prenatal diagnosis among Greek women: a national survey

Prenatal diagnosis, 1998-04, Vol.18 (4), p.349-355

1998

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Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-[epsilon] Antibody

Fetal diagnosis and therapy, 2003-09, Vol.18 (5), p.309

2003

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Use of Annexin V Antibody to Identify Apoptotic Cells during Pregnancy

Annals of the New York Academy of Sciences, 2001-09, Vol.945 (1), p.145-150

2001

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3' Acceptor splice site mutation in intron 50 leads to mild Duchenne muscular dystrophy phenotype

Human mutation, 1998, Vol.Suppl 1, p.S209-S212

1998

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22q11 microdeletion syndrome

Pediatric research, 1999-06, Vol.45 (6), p.919-919

1999

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Deletion patterns of Duchenne and Becker muscular dystrophies in Greece

Journal of medical genetics, 1995-01, Vol.32 (1), p.48-51

1995

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Evidence for Reduced Recombination on the Nondisjoined Chromosomes 21 in Down Syndrome

Science (American Association for the Advancement of Science), 1987-08, Vol.237 (4815), p.652-654

1987

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A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation

Clinical genetics, 1983-11, Vol.24 (5), p.380-383

1983

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3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype

Human mutation, 1998, Vol.11 (S1), p.S209-S212

1998

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Prenatal diagnosis of chromosomal abnormalities from chorionic biopsy samples: Improved success rate using a modified direct method

Prenatal diagnosis, 1987-09, Vol.7 (7), p.461-469

1987

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Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings: FISH on PB of CML patients

Clinical and laboratory haematology, 2002-12, Vol.24 (6), p.361-367

2002

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Polymorphism of chromosome 9 in 600 Greek subjects

American journal of human genetics, 1978-01, Vol.30 (1), p.85-89

1978

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10 Years' Experience in Fragile X Testing Among Mentally Retarded Individuals in Greece: A Molecular and Epidemiological Approach

Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-ε Antibody

Cohen syndrome : two new cases in siblings

Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings

Identification of three polymorphisms in the dystrophin gene

Prenatal Diagnosis Services in Greece

Chromosome fragility and predisposition to childhood malignancies

Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol

De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia

Analysis of DNA Haplotypes Suggests a Genetic Predisposition to Trisomy 21 Associated with DNA Sequences on Chromosome 21

Detection of Fetal NRBCs in Maternal Blood of Pregnant Carriers of β-Thalassemia Using Anti-γ and Anti-ε Monoclonal Antibodies

A 10-YEAR EXPERIENCE OF MOLECULAR TESTING IN DMD/BMD MUSCULAR DYSTROPHIES IN GREECE

The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphisms

Awareness and use of prenatal diagnosis among Greek women: a national survey

Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-[epsilon] Antibody

Use of Annexin V Antibody to Identify Apoptotic Cells during Pregnancy

3' Acceptor splice site mutation in intron 50 leads to mild Duchenne muscular dystrophy phenotype

22q11 microdeletion syndrome

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece

Evidence for Reduced Recombination on the Nondisjoined Chromosomes 21 in Down Syndrome

A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation

3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype

Prenatal diagnosis of chromosomal abnormalities from chorionic biopsy samples: Improved success rate using a modified direct method

Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings: FISH on PB of CML patients

Polymorphism of chromosome 9 in 600 Greek subjects

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