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The sacral autonomic outflow is sympathetic

Science (American Association for the Advancement of Science), 2016-11, Vol.354 (6314), p.893-897

2016

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Parasympathetic ganglia derive from Schwann cell precursors

Science (American Association for the Advancement of Science), 2014-07, Vol.345 (6192), p.87-90

2014

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Ventilatory response to hyperoxia in newborn mice heterozygous for the transcription factor Phox2b

American journal of physiology. Regulatory, integrative and comparative physiology, 2006-06, Vol.290 (6), p.R1691-R1696

2006

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Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21

European journal of human genetics : EJHG, 1993, Vol.1 (2), p.114-124

1993

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The sacral autonomie outflow is sympathetic

Science (American Association for the Advancement of Science), 2016-11, Vol.354 (6314), p.893-897

2016

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Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1989-08, Vol.86 (15), p.5958-5962

1989

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Transgenic Mouse In Vivo Library of Human Down Syndrome Critical Region 1: Association between DYRK1A Overexpression, Brain Development Abnormalities, and Cell Cycle Protein Alteration

Journal of neuropathology and experimental neurology, 2004-05, Vol.63 (5), p.429-440

2004

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Mapping of the down syndrome phenotype on chromosome 21 at the molecular level

Biomedicine & pharmacotherapy, 1994, Vol.48 (5), p.247-252

1994

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Neurodevelopment. Parasympathetic ganglia derive from Schwann cell precursors

Science (American Association for the Advancement of Science), 2014-07, Vol.345 (6192), p.87-90

2014

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The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice

Biochemical and biophysical research communications, 2003-06, Vol.305 (4), p.915-924

2003

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Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21

American journal of human genetics, 1990-03, Vol.46 (3), p.518-526

1990

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Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region

American journal of human genetics, 1995-07, Vol.57 (1), p.62-71

1995

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Molecular mapping of 21 features associated with partial monosomy 21 : involvement of the APP-SODI region

American journal of human genetics, 1995, Vol.57 (1), p.62-71

1995

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135 Effet de la température ambiante sur la réponse ventilatoire au CO2 des souriceaux hétérozygotes pour le facteur de transcription Phox2b

Revue des maladies respiratoires, 2006-11, Vol.23 (5), p.584-584

2006

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Direct electronic radioisotope detection yields improved gene dosage analysis

BioTechniques, 1990-08, Vol.9 (2), p.162

1990

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C21orf5, a Novel Human Chromosome 21 Gene, Has a Caenorhabditis elegans Ortholog (pad-1) Required for Embryonic Patterning

Genomics (San Diego, Calif.), 2000-08, Vol.68 (1), p.30-40

2000

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Molecular mapping of the Down syndrome phenotype on chromosome 21

Progress in clinical and biological research, 1993, Vol.384, p.63

1993

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Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome

Genomics (San Diego, Calif.), 1998-02, Vol.48 (1), p.12-23

1998

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3.6-Mb Genomic and YAC Physical Map of the Down Syndrome Chromosome Region on Chromosome 21

Genomics (San Diego, Calif.), 1994-02, Vol.19 (3), p.462-469

1994

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No significant effect of monosomy for distal 21q22.3 on the down syndrome phenotype in Mirror duplications of chromosome 21

American journal of human genetics, 1992-12, Vol.51 (6), p.1240-1250

1992

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Down syndrome critical region around D21S55 on proximal 21q22.3

American journal of medical genetics, 1990, Vol.37 (S7), p.98-103

1990

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3. 6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21

Genomics (San Diego, Calif.), 1994-02, Vol.19:3

1994

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Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level : Human genetics

Biomedicine & pharmacotherapy, 1994, Vol.48 (5-6), p.247-252

1994

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No significant effect of monosomy for distal 21q22. 3 on the Down syndrom phenotype in mirror' duplications of chromosome 21

American journal of human genetics, 1992-12, Vol.51:6

1992

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Gene-dosage mapping of 30 DNA markers on chromosome 21

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.887-889

1992

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The sacral autonomic outflow is sympathetic

Parasympathetic ganglia derive from Schwann cell precursors

Ventilatory response to hyperoxia in newborn mice heterozygous for the transcription factor Phox2b

Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21

The sacral autonomie outflow is sympathetic

Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome

Transgenic Mouse In Vivo Library of Human Down Syndrome Critical Region 1: Association between DYRK1A Overexpression, Brain Development Abnormalities, and Cell Cycle Protein Alteration

Mapping of the down syndrome phenotype on chromosome 21 at the molecular level

Neurodevelopment. Parasympathetic ganglia derive from Schwann cell precursors

The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice

Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region

Molecular mapping of 21 features associated with partial monosomy 21 : involvement of the APP-SODI region

135 Effet de la température ambiante sur la réponse ventilatoire au CO2 des souriceaux hétérozygotes pour le facteur de transcription Phox2b

Direct electronic radioisotope detection yields improved gene dosage analysis

C21orf5, a Novel Human Chromosome 21 Gene, Has a Caenorhabditis elegans Ortholog (pad-1) Required for Embryonic Patterning

Molecular mapping of the Down syndrome phenotype on chromosome 21

Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome

3.6-Mb Genomic and YAC Physical Map of the Down Syndrome Chromosome Region on Chromosome 21

No significant effect of monosomy for distal 21q22.3 on the down syndrome phenotype in Mirror duplications of chromosome 21

Down syndrome critical region around D21S55 on proximal 21q22.3

3. 6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21

Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level : Human genetics

No significant effect of monosomy for distal 21q22. 3 on the Down syndrom phenotype in mirror' duplications of chromosome 21

Gene-dosage mapping of 30 DNA markers on chromosome 21

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