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P Monaco

Showing results (531-540 of 719) with videos related to

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American Journal of Medical Genetics|September 22, 1999
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism ConsortiumE Maestrini, C Lai, A Marlow, et al.
Molecular Psychiatry|October 25, 2007
Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populationsC Toma, M Rossi, I Sousa, et al.
The Journal of Bone and Joint Surgery. British Volume|September 28, 2004
Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype studyD E Porter, L Lonie, M Fraser, et al.
Transplantation|November 30, 2005
Intensive care unit extubation does not preclude extrarenal organ recovery from donors after cardiac deathScott R Johnson, Martha Pavlakis, Khalid Khwaja, et al.
Lancet (London, England)|January 27, 1973
Influence of rejection therapy on fungal and nocardial infections in renal-transplant recipientsM C Bach, J L Adler, J Breman, et al.
Human Molecular Genetics|August 1, 1997
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 geneY Ishikawa-Brush, J F Powell, P Bolton, et al.
Nucleic Acids Research|May 25, 1991
Molecular cloning and analysis of the fragile X region in manA Dietrich, P Kioschis, A P Monaco, et al.
Human Molecular Genetics|August 1, 1993
2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genesR G Lafrenière, C J Brown, S Rider, et al.
Science (New York, N.Y.)|October 2, 1992
Genome maps III. 1992. Wall ChartJ L Mandel, A P Monaco, D L Nelson, et al.
Human Genetics|December 24, 2025
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genesKrzysztof Marianski, Joel B Talcott, John Stein, et al.
Pageof 72

Showing results (531-540 of 719) with videos related to

Sort By:
Pageof 72
American Journal of Medical Genetics|September 22, 1999
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism ConsortiumE Maestrini, C Lai, A Marlow, et al.
Molecular Psychiatry|October 25, 2007
Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populationsC Toma, M Rossi, I Sousa, et al.
The Journal of Bone and Joint Surgery. British Volume|September 28, 2004
Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype studyD E Porter, L Lonie, M Fraser, et al.
Transplantation|November 30, 2005
Intensive care unit extubation does not preclude extrarenal organ recovery from donors after cardiac deathScott R Johnson, Martha Pavlakis, Khalid Khwaja, et al.
Lancet (London, England)|January 27, 1973
Influence of rejection therapy on fungal and nocardial infections in renal-transplant recipientsM C Bach, J L Adler, J Breman, et al.
Human Molecular Genetics|August 1, 1997
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 geneY Ishikawa-Brush, J F Powell, P Bolton, et al.
Nucleic Acids Research|May 25, 1991
Molecular cloning and analysis of the fragile X region in manA Dietrich, P Kioschis, A P Monaco, et al.
Human Molecular Genetics|August 1, 1993
2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genesR G Lafrenière, C J Brown, S Rider, et al.
Science (New York, N.Y.)|October 2, 1992
Genome maps III. 1992. Wall ChartJ L Mandel, A P Monaco, D L Nelson, et al.
Human Genetics|December 24, 2025
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genesKrzysztof Marianski, Joel B Talcott, John Stein, et al.
Pageof 72