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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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Analyse par FISH interphasique de tissus congelés ou fixés pour la détection de la t(11;14)(q13;q32) dans les lymphomes du manteau

Morphologie, 2001, Vol.85 (270), p.15-22

2001

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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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An adaptive blocking strategy for matrix factorizations

CONPAR 90 — VAPP IV, 1990, Vol.457, p.210-221

1990

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Interphase FISH analysis on histologic sections of fixed tissues for t(11;14) (q13;q32) detection in mantle cell lymphoma and t(8;14)(q24;q32) in Burkitt's lymphoma

Annales de pathologie, 2002-04, Vol.22 (2), p.145-149

2002

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Interphase FISH analysis of frozen or fixed tissues for the detection of t(11;14) (q13;q32) in mantle cell lymphoma

Morphologie, 2001-09, Vol.85 (270), p.15-22

2001

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Primary angioplasty versus prehospital fibrinolysis in acute myocardial infarction: a randomised study

The Lancet (British edition), 2002-09, Vol.360 (9336), p.825-829

2002

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Architecture of the human regulatory network derived from ENCODE data

Nature (London), 2012-09, Vol.489 (7414), p.91-100

2012

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Olmesartan‐associated enteropathy: results of a national survey

Alimentary pharmacology & therapeutics, 2014-11, Vol.40 (9), p.1103-1109

2014

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A global reference for human genetic variation

Nature (London), 2015-10, Vol.526 (7571), p.68-74

2015

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Dissection of Dom34-Hbs1 reveals independent functions in two RNA quality control pathways

Nature structural & molecular biology, 2010-12, Vol.17 (12), p.1446

2010

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Comparison of primary angioplasty and pre-hospital fibrinolysis in acute myocardial infarction (CAPTIM) trial: a 5-year follow-up

European heart journal, 2009-07, Vol.30 (13), p.1598-1606

2009

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An integrated encyclopedia of DNA elements in the human genome

Nature (London), 2012-09, Vol.489 (7414), p.57-74

2012

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An integrated map of genetic variation from 1,092 human genomes

Nature (London), 2012-11, Vol.491 (7422), p.56-65

2012

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A user's guide to the encyclopedia of DNA elements (ENCODE)

PLoS biology, 2011-04, Vol.9 (4), p.e1001046-e1001046

2011

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Squeezing the Optical Near-Field Zone by Plasmon Coupling of Metallic Nanoparticles

Physical review letters, 1999-03, Vol.82 (12), p.2590-2593

1999

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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature communications, 2014-06, Vol.5 (1), p.3934-3934, Article 3934

2014

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Diversity of Human Copy Number Variation and Multicopy Genes

Science (American Association for the Advancement of Science), 2010-10, Vol.330 (6004), p.641-646

2010

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Mapping copy number variation by population-scale genome sequencing

Nature (London), 2011-02, Vol.470 (7332), p.59-65

2011

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Imaging the local density of states of optical corrals

Physical review letters, 2002-03, Vol.88 (9), p.097402-097402, Article 097402

2002

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Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences

Genome biology, 2014-06, Vol.15 (6), p.R88-R88

2014

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Is primary angioplasty more effective than prehospital fibrinolysis in diabetics with acute myocardial infarction? Data from the CAPTIM randomized clinical trial

European heart journal, 2005-09, Vol.26 (17), p.1712-1718

2005

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The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2023-01, Vol.23 (1), p.48-56

2023

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Dysregulation of laminins in intestinal inflammation

Pathologie biologie (Paris), 2012-02, Vol.60 (1), p.41-47

2012

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Subwavelength mapping of surface photonic states

Nanotechnology, 2003-08, Vol.14 (8), p.935-938

2003

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

Analyse par FISH interphasique de tissus congelés ou fixés pour la détection de la t(11;14)(q13;q32) dans les lymphomes du manteau

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

An adaptive blocking strategy for matrix factorizations

Interphase FISH analysis on histologic sections of fixed tissues for t(11;14) (q13;q32) detection in mantle cell lymphoma and t(8;14)(q24;q32) in Burkitt's lymphoma

Interphase FISH analysis of frozen or fixed tissues for the detection of t(11;14) (q13;q32) in mantle cell lymphoma

Primary angioplasty versus prehospital fibrinolysis in acute myocardial infarction: a randomised study

Architecture of the human regulatory network derived from ENCODE data

Olmesartan‐associated enteropathy: results of a national survey

A global reference for human genetic variation

Dissection of Dom34-Hbs1 reveals independent functions in two RNA quality control pathways

Comparison of primary angioplasty and pre-hospital fibrinolysis in acute myocardial infarction (CAPTIM) trial: a 5-year follow-up

An integrated encyclopedia of DNA elements in the human genome

An integrated map of genetic variation from 1,092 human genomes

A user's guide to the encyclopedia of DNA elements (ENCODE)

Squeezing the Optical Near-Field Zone by Plasmon Coupling of Metallic Nanoparticles

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Diversity of Human Copy Number Variation and Multicopy Genes

Mapping copy number variation by population-scale genome sequencing

Imaging the local density of states of optical corrals

Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences

Is primary angioplasty more effective than prehospital fibrinolysis in diabetics with acute myocardial infarction? Data from the CAPTIM randomized clinical trial

The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis

Dysregulation of laminins in intestinal inflammation

Subwavelength mapping of surface photonic states

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