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Discordant sex in monozygotic XXY/XX twins: a case report

Human reproduction (Oxford), 2014-12, Vol.29 (12), p.2814-2820

2014

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Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia

Leukemia, 2009-01, Vol.23 (1), p.125-133

2009

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5-HT4 Receptors: Cloning and Expression of New Splice Variants

Annals of the New York Academy of Sciences, 1998-12, Vol.861 (1), p.49-56

1998

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The human growth factor-inducible immediate early gene, CYR61, maps to chromosome 1p

Oncogene, 1997-04, Vol.14 (14), p.1753-1757

1997

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Human E2F5 gene is oncogenic in primary rodent cells and is amplified in human breast tumors

Genes chromosomes & cancer, 2000-05, Vol.28 (1), p.126-130

2000

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The Human SOX11 Gene: Cloning, Chromosomal Assignment and Tissue Expression

Genomics (San Diego, Calif.), 1995-09, Vol.29 (2), p.541-545

1995

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What Are the Causes for Failures of Primary Hip Arthroplasties in France?

Clinical orthopaedics and related research, 2013-12, Vol.471 (12), p.3863-3869

2013

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Revelation of an acute lymphoblastic leukemia in the delivery room

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2007-07, Vol.14 (7), p.887-889

2007

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PC8 [corrected], a new member of the convertase family

Biochemical journal, 1996-03, Vol.314 ( Pt 3) (3), p.727-731

1996

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Leucémie aiguë lymphoblastique néonatale : une affection rare à révélation immédiate en salle de naissance

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2007-07, Vol.14 (7), p.887-889

2007

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Localization of Staf50, a member of the ring finger family, to 11p15 by fluorescence in situ hybridization

Genomics (San Diego, Calif.), 1996-05, Vol.34 (1), p.151-153

1996

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Expression and Human Chromosomal Localization to 17q25 of the Growth-Regulated Gene Encoding the Mitochondrial Ribosomal Protein MRPL12

Genomics (San Diego, Calif.), 1997-05, Vol.41 (3), p.453-457

1997

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Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases

Genes chromosomes & cancer, 2003-11, Vol.38 (3), p.234-239

2003

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Localization of Human Cell Cycle Regulatory Genes CDC25C to 5q31 and WEE1 to 11p15.3-11p15.1 by Fluorescence in Situ Hybridization

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.194-196

1993

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A randomized study of pegylated liposomal doxorubicin versus continuous-infusion doxorubicin in elderly patients with acute lymphoblastic leukemia: the GRAALL-SA1 study

Haematologica (Roma), 2011-02, Vol.96 (2), p.245-252

2011

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Distribution of olfactory receptor genes in the human genome

Nature genetics, 1998-03, Vol.18 (3), p.243-250

1998

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The human necdin gene, NDN , is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Nature genetics, 1997-11, Vol.17 (3), p.357-361

1997

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Localization of the ribonuclease L inhibitor gene (RNSAI), a new member of the interferon-regulated 2-5A pathway, to 4q31 by fluorescence in situ hybridization

Genomics (San Diego, Calif.), 1996-03, Vol.32 (3), p.488-490

1996

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Assignment of 5-hydroxytryptamine receptor (HTR4) to human chromosome 5 bands q31-->q33 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.78 (2), p.133-134

1997

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Assignment of human genes for β2 and β4 subunits of voltage-dependent Ca2+ channels to chromosomes 10p12 and 2q22-q23

Human genetics, 1997-07, Vol.100 (2), p.151-154

1997

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Chromosomal localization of the human genes for α1A, α1B, and α1E voltage-dependent Ca2+ channel subunits

Genomics (San Diego, Calif.), 1995-12, Vol.30 (3), p.605-609

1995

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Assignment of TRIO, the Trio gene (PTPRF interacting) to human chromosome bands 5p15.1→p14 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.76 (1-2), p.107-108

1997

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Assignment of thyroid hormone responsive SPOT 14 homolog (THRSP) to human chromosome 11 bands q13.5-->q14.1 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.76 (3-4), p.219-220

1997

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Localization of ARHG, a Member of the RAS Homolog Gene Family, to 11p15.5-11p15.4 by Fluorescence in Situ Hybridization

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.788-790

1993

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Discordant sex in monozygotic XXY/XX twins: a case report

Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia

5-HT4 Receptors: Cloning and Expression of New Splice Variants

The human growth factor-inducible immediate early gene, CYR61, maps to chromosome 1p

Human E2F5 gene is oncogenic in primary rodent cells and is amplified in human breast tumors

The Human SOX11 Gene: Cloning, Chromosomal Assignment and Tissue Expression

What Are the Causes for Failures of Primary Hip Arthroplasties in France?

Revelation of an acute lymphoblastic leukemia in the delivery room

PC8 [corrected], a new member of the convertase family

Leucémie aiguë lymphoblastique néonatale : une affection rare à révélation immédiate en salle de naissance

Localization of Staf50, a member of the ring finger family, to 11p15 by fluorescence in situ hybridization

Expression and Human Chromosomal Localization to 17q25 of the Growth-Regulated Gene Encoding the Mitochondrial Ribosomal Protein MRPL12

Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases

Localization of Human Cell Cycle Regulatory Genes CDC25C to 5q31 and WEE1 to 11p15.3-11p15.1 by Fluorescence in Situ Hybridization

Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH)

A randomized study of pegylated liposomal doxorubicin versus continuous-infusion doxorubicin in elderly patients with acute lymphoblastic leukemia: the GRAALL-SA1 study

Distribution of olfactory receptor genes in the human genome

The human necdin gene, NDN , is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Localization of the ribonuclease L inhibitor gene (RNSAI), a new member of the interferon-regulated 2-5A pathway, to 4q31 by fluorescence in situ hybridization

Assignment of 5-hydroxytryptamine receptor (HTR4) to human chromosome 5 bands q31-->q33 by in situ hybridization

Assignment of human genes for β2 and β4 subunits of voltage-dependent Ca2+ channels to chromosomes 10p12 and 2q22-q23

Chromosomal localization of the human genes for α1A, α1B, and α1E voltage-dependent Ca2+ channel subunits

Assignment of TRIO, the Trio gene (PTPRF interacting) to human chromosome bands 5p15.1→p14 by in situ hybridization

Assignment of thyroid hormone responsive SPOT 14 homolog (THRSP) to human chromosome 11 bands q13.5-->q14.1 by in situ hybridization

Localization of ARHG, a Member of the RAS Homolog Gene Family, to 11p15.5-11p15.4 by Fluorescence in Situ Hybridization

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