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Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia

Andrologia, 2015-02, Vol.47 (1), p.112-115

2015

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A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES

Genetic counseling, 2016, Vol.27 (1), p.51

2016

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PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH

Genetic counseling, 2015-01, Vol.26 (3), p.299

2015

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PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)

Genetic counseling, 2015-01, Vol.26 (2), p.243

2015

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22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2)

Genetic counseling, 2015, Vol.26 (1), p.67

2015

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A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONS

Genetic counseling, 2015-01, Vol.26 (3), p.347

2015

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Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

Balkan journal of medical genetics, 2011-01, Vol.14 (1), p.57-60

2011

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Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype

Genetic counseling, 2011-01, Vol.22 (2), p.199

2011

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Aplasia Ras Homologous Member I Gene and Development of Glial Tumors

Balkan journal of medical genetics, 2011-01, Vol.14 (1), p.37-43

2011

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De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome

Genetic counseling, 2011, Vol.22 (1), p.63

2011

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Retinoic acid isomers protect hippocampal neurons from amyloid-beta induced neurodegeneration

Neurotoxicity research, 2005, Vol.7 (3), p.243-250

2005

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Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16

Genetic counseling, 2009-01, Vol.20 (4), p.327

2009

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Novel cytogenetic findings revealed by conventional cytogenetic and FISH analyses in leukaemia patients

Experimental oncology, 2005-09, Vol.27 (3), p.229

2005

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Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features

Genetic counseling, 2005, Vol.16 (2), p.129

2005

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Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate

Genetic counseling, 2007-01, Vol.18 (2), p.163

2007

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Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications

Journal of medical genetics, 2000-04, Vol.37 (4), p.281-286

2000

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Evaluation of Complex Inheritance Involving the Most Common Bardet-Biedl Syndrome Locus ( BBS1)

American journal of human genetics, 2003-02, Vol.72 (2), p.429-437

2003

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Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages

Clinical genetics, 2002-01, Vol.61 (1), p.26-31

2002

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Differential PTEN Protein Expression Profiles in Superficial versus Invasive Bladder Cancers

Urologia internationalis, 2005-01, Vol.75 (2), p.102-106

2005

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A case with de novo interstitial deletion of chromosome 7q21.1-q22

Genetic counseling, 2005, Vol.16 (2), p.155

2005

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A rare case of Turner's Syndrome with 45, X/46, X, Dic (X) (qter→p11.1::p11.4→qter)

Hereditas, 1990-01, Vol.113 (3), p.217-220

1990

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M-FISH applications in clinical genetics

Genetic counseling, 2005, Vol.16 (3), p.257

2005

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Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia

Andrologia, 2015, Vol.47 (1), p.112-115

2015

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Existence of acute lymphoblastic leukemia and osteosarcoma in a child

Journal of pediatric hematology/oncology, 2002-10, Vol.24 (7), p.572-574

2002

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Cytogenetic Findings in Thirty Lung Carcinoma Patients

Cancer genetics and cytogenetics, 1998-01, Vol.100 (2), p.114-123

1998

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Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia

A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES

PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH

PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)

22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2)

A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONS

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype

Aplasia Ras Homologous Member I Gene and Development of Glial Tumors

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome

Retinoic acid isomers protect hippocampal neurons from amyloid-beta induced neurodegeneration

Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16

Novel cytogenetic findings revealed by conventional cytogenetic and FISH analyses in leukaemia patients

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features

Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications

Evaluation of Complex Inheritance Involving the Most Common Bardet-Biedl Syndrome Locus ( BBS1)

Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages

Differential PTEN Protein Expression Profiles in Superficial versus Invasive Bladder Cancers

A case with de novo interstitial deletion of chromosome 7q21.1-q22

A rare case of Turner's Syndrome with 45, X/46, X, Dic (X) (qter→p11.1::p11.4→qter)

M-FISH applications in clinical genetics

Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia

Existence of acute lymphoblastic leukemia and osteosarcoma in a child

Cytogenetic Findings in Thirty Lung Carcinoma Patients

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