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Angiogenesis as a prognostic marker in breast carcinoma with conventional adjuvant chemotherapy: a multiparametric and immunohistochemical analysis

The Journal of pathology, 1998-02, Vol.184 (2), p.130-135

1998

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Sperm analysis by FISH in a case of t(17; 22) (q11; q12) balanced translocation: Case report

Human reproduction (Oxford), 2002-02, Vol.17 (2), p.325-331

2002

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De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder

Genetic counseling, 2006, Vol.17 (3), p.371

2006

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An unusual familial chromosome 9 “variant” with variable phenotype: characterization by CGH analysis

Morphologie, 2005-06, Vol.89 (285), p.71-75

2005

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A fetus with pseudo Fryns syndrome and t(18;22) translocation

Genetic counseling, 2001, Vol.12 (2), p.169

2001

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Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X :Y translocation in a patient with secondary amenorrhoea

Molecular human reproduction, 1997-05, Vol.3 (5), p.439-443

1997

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Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesis

Prenatal diagnosis, 1994-04, Vol.14 (4), p.303-306

1994

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A history of miscarriages and mild prognathism as possible mode of presentation of mosaic trisomy 18 in women

Clinical genetics, 1996-12, Vol.50 (6), p.470-473

1996

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Sperm analysis by FISH in a case of t(17; 22) (qll; q12) balanced translocation

Human reproduction (Oxford), 2002-02, Vol.17 (2), p.325-331

2002

Volltextzugriff (PDF)

A Case Report of Down Syndrome and Centroblastic Lymphoma

Pathology, research and practice, 1996-12, Vol.192 (12), p.1266-1269

1996

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Chromosome analysis by image processing in a computerized environment. Clinical applications

Journal of radiation research, 1992, Vol.33 Suppl (SUPPLEMENT), p.171-188

1992

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Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis

Prenatal diagnosis, 2004-04, Vol.24 (4), p.249-256

2004

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Recent advances in image treatment for chromosome analysis

Genetics selection evolution (Paris), 1991-08, Vol.23 (Suppl 1), p.S57-S63, Article S57

1991

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Un Système Interactif d'Analyse Chromosomique

CYTOLOGIA, 1988/09/25, Vol.53(3), pp.509-515

1988

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Diagnostic prénatal rapide par hybridation in situ fluorescente chez les fœtus de parents remaniés

Morphologie, 2006-06, Vol.90 (289), p.82-82

2006

Volltextzugriff (PDF)

An interactive system of chromosome analysis

Cytologia, 1988, Vol.53 (3), p.509-515

1988

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Aspects of intracranial and spinal tumors in patients with Down syndrome and report of a rapidly progressing Grade 2 astrocytoma

Cancer, 2001-04, Vol.91 (8), p.1458-1466

2001

Volltextzugriff (PDF)

Apport des Techniques de Cytogénétique Appliquées aux Cellules des Liquides d'Epanchement dans le Depistage de la Malignité

CYTOLOGIA, 1985/06/25, Vol.50(2), pp.323-331

1985

Volltextzugriff (PDF)

Chromosomal banding by the action of two compounds: sodium glycocholate and arginine

Biology of the cell, 1985, Vol.53 (1), p.89-91

1985

Volltextzugriff (PDF)

Another reason to look for tumor suppressor genes on chromosome 21

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

1998

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Interchromosomal fibers: human ultrastructural study by a recent technique

Human genetics, 1974-01, Vol.25 (2), p.119-126

1974

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Chromosomal aberrations in a case of acute myelomonocytic leukemia (M4)

Pathologica, 1987-09, Vol.79 (1063), p.593

1987

Volltextzugriff (PDF)

Évaluation du taux d’aberrations chromosomiques dans les spermatozoïdes de sujets présentant une anomalie du caryotype

Morphologie, 2004-07, Vol.88 (281), p.107-107

2004

Volltextzugriff (PDF)

Recent advances in image treatment for chromosome analysis

Genetics selection evolution (Paris), 1991, Vol.23 (Suppl1), p.57s-63s

1991

Volltextzugriff (PDF)

Duplication of part of the short arm of A1 in a case of erythroleukemia (M6)

Pathologica, 1985-09, Vol.77 (1051), p.563

1985

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Angiogenesis as a prognostic marker in breast carcinoma with conventional adjuvant chemotherapy: a multiparametric and immunohistochemical analysis

Sperm analysis by FISH in a case of t(17; 22) (q11; q12) balanced translocation: Case report

De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder

An unusual familial chromosome 9 “variant” with variable phenotype: characterization by CGH analysis

A fetus with pseudo Fryns syndrome and t(18;22) translocation

Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X :Y translocation in a patient with secondary amenorrhoea

Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesis

A history of miscarriages and mild prognathism as possible mode of presentation of mosaic trisomy 18 in women

Sperm analysis by FISH in a case of t(17; 22) (qll; q12) balanced translocation

A Case Report of Down Syndrome and Centroblastic Lymphoma

Chromosome analysis by image processing in a computerized environment. Clinical applications

Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis

Recent advances in image treatment for chromosome analysis

Un Système Interactif d'Analyse Chromosomique

Diagnostic prénatal rapide par hybridation in situ fluorescente chez les fœtus de parents remaniés

An interactive system of chromosome analysis

Aspects of intracranial and spinal tumors in patients with Down syndrome and report of a rapidly progressing Grade 2 astrocytoma

Apport des Techniques de Cytogénétique Appliquées aux Cellules des Liquides d'Epanchement dans le Depistage de la Malignité

Chromosomal banding by the action of two compounds: sodium glycocholate and arginine

Another reason to look for tumor suppressor genes on chromosome 21

Interchromosomal fibers: human ultrastructural study by a recent technique

Chromosomal aberrations in a case of acute myelomonocytic leukemia (M4)

Évaluation du taux d’aberrations chromosomiques dans les spermatozoïdes de sujets présentant une anomalie du caryotype

Recent advances in image treatment for chromosome analysis

Duplication of part of the short arm of A1 in a case of erythroleukemia (M6)

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