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New chromosomal syndromes

Pathologie biologie (Paris), 2008-09, Vol.56 (6), p.380-387

2008

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Analysis of cell‐free fetal DNA in maternal blood for detection of trisomy 21, 18 and 13 in a general pregnant population and in a high risk population – a systematic review and meta‐analysis

Acta obstetricia et gynecologica Scandinavica, 2017-01, Vol.96 (1), p.7-18

2017

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Pitfalls and update in haematopathology. Case 6. B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma

Annales de pathologie, 2012-10, Vol.32 (5), p.356-362

Moreau, Anne

2012

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Genetic abnormalities in multiple myeloma: role in oncogenesis and impact on survival

La revue de medecine interne, 2007-10, Vol.28 (10), p.677-681

2007

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Pulmonary synovial sarcoma: case study and literature review

The Pan African medical journal, 2020-06, Vol.36, p.137

2020

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Retinal abnormalities in three genetic disorders involving the X chromosome

Journal francais d'ophtalmologie, 2020-12, Vol.43 (10), p.1107

2020

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Dermatofibrosarcoma: Management

Bulletin du cancer, 2018-11, Vol.105 (11), p.1094-1101

2018

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Perspectives: FISH on cytological samples

Annales de pathologie, 2011-11, Vol.31 (5 Suppl), p.S103-S104

Courtade-Saïdi, Monique

2011

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Study of Siberian population movements: use of multiple markers

Bulletin de l'Académie nationale de médecine, 2012-06, Vol.196 (6), p.1087-1100; discussion 1100-2

Ludes, Bertrand

2012

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Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2

Clinical genetics, 2009-03, Vol.75 (3), p.259-264

2009

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Establishing transcriptional silencing of the X chromosome during early embryogenesis

Biologie aujourd'hui, 2010, Vol.204 (3), p.199

2010

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Genetic and clinical aspects of lissencephaly

Revue neurologique, 2007-05, Vol.163 (5), p.533

2007

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Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes

American journal of human genetics, 2007-09, Vol.81 (3), p.475-491

2007

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Chronic myeloid leukemia with variant e19a2 BCR-ABL1 fusion transcript: interest of the molecular identification at diagnosis for minimal residual disease follow-up

Annales de biologie clinique (Paris), 2014-05, Vol.72 (3), p.359-366

2014

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Will genetics allow for the differentiation of schizophrenia and maniac-depressive psychosis?

Encéphale, 2005-02, Vol.31 (Pt 2), p.S23-S27

2005

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Hemophagocytic lymphohistiocytosis associated with a lymphohistiocytic pattern anaplastic large cell lymphoma: a case report

Annales de pathologie, 2013-08, Vol.33 (4), p.278-282

2013

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Keratinisation disorders: new data

Annales de dermatologie et de vénéréologie, 2013-02, Vol.140 (2), p.150-151

Dereure, O

2013

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From cytogenetics to cytogenomics of adipose tissue tumors: 1. Benign adipose tissue tumors

Bulletin du cancer, 2002-07, Vol.89 (7-8), p.689

2002

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Pitfalls and update in Haematopathology. Case 1. Follicular lymphoma grade 1-2 according to the WHO classification 2008, "pseudo BCL2 negative" with low and heterogeneous expression of the CD10

Annales de pathologie, 2012-10, Vol.32 (5), p.331-335

Copie-Bergman, Christiane

2012

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ALK+ diffuse large B-cell lymphoma

Annales de pathologie, 2012-10, Vol.32 (5), p.351-355

Parrens, Marie

2012

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The end of sexual dimorphism is programmed?

Revue médicale suisse, 2011-02, Vol.7 (283), p.463

2011

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BCL11A controls the expression of the human fetal hemoglobin

M.S. Médecine sciences, 2012-11, Vol.28 (11), p.923

Labie, Dominique

2012

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Pitfalls and update in haematopathology. Case 2. "Early phase" mantle cell lymphoma of the lymph node

Annales de pathologie, 2012-10, Vol.32 (5), p.336-340

Copie-Bergman, Christiane

2012

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Genes and environment in susceptibility to visceral leishmaniasis

Comptes rendus. Biologies, 2006-11, Vol.329 (11), p.863-870

2006

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A cytological, immunophenotypical and cytogenetical study of 136 consecutive cases of B-cell chronic lymphoid hemopathies

Pathologie biologie (Paris), 2007-02, Vol.55 (1), p.59-72

2007

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New chromosomal syndromes

Analysis of cell‐free fetal DNA in maternal blood for detection of trisomy 21, 18 and 13 in a general pregnant population and in a high risk population – a systematic review and meta‐analysis

Pitfalls and update in haematopathology. Case 6. B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma

Genetic abnormalities in multiple myeloma: role in oncogenesis and impact on survival

Pulmonary synovial sarcoma: case study and literature review

Retinal abnormalities in three genetic disorders involving the X chromosome

Dermatofibrosarcoma: Management

Perspectives: FISH on cytological samples

Study of Siberian population movements: use of multiple markers

Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2

Establishing transcriptional silencing of the X chromosome during early embryogenesis

Genetic and clinical aspects of lissencephaly

Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes

Chronic myeloid leukemia with variant e19a2 BCR-ABL1 fusion transcript: interest of the molecular identification at diagnosis for minimal residual disease follow-up

Will genetics allow for the differentiation of schizophrenia and maniac-depressive psychosis?

Hemophagocytic lymphohistiocytosis associated with a lymphohistiocytic pattern anaplastic large cell lymphoma: a case report

Keratinisation disorders: new data

From cytogenetics to cytogenomics of adipose tissue tumors: 1. Benign adipose tissue tumors

Pitfalls and update in Haematopathology. Case 1. Follicular lymphoma grade 1-2 according to the WHO classification 2008, "pseudo BCL2 negative" with low and heterogeneous expression of the CD10

ALK+ diffuse large B-cell lymphoma

The end of sexual dimorphism is programmed?

BCL11A controls the expression of the human fetal hemoglobin

Pitfalls and update in haematopathology. Case 2. "Early phase" mantle cell lymphoma of the lymph node

Genes and environment in susceptibility to visceral leishmaniasis

A cytological, immunophenotypical and cytogenetical study of 136 consecutive cases of B-cell chronic lymphoid hemopathies

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