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M Justice

Showing results (221-230 of 254) with videos related to

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Genes|September 23, 2022
<i>TBX3</i> and <i>EFNA4</i> Variant in a Family with Ulnar-Mammary Syndrome and Sagittal CraniosynostosisMoon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, et al.
BMC Proceedings|March 1, 2012
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence dataClaire L Simpson, Cristina M Justice, Mera Krishnan, et al.
International Forum of Allergy & Rhinology|April 11, 2025
Silastic Septal Splints in the Management of Refractory Epistaxis in Hereditary Hemorrhagic TelangiectasiaAvraham Adelman, Eunice Im, Brett Labella, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32Nancy H Miller, Beth Marosy, Cristina M Justice, et al.
Blood Vessels, Thrombosis & Hemostasis|October 16, 2025
Nasal RADA16 hydrogel application decreases epistaxis severity scores in adults with hereditary hemorrhagic telangiectasiaAvraham Adelman, Eunice Im, Lindsey Jackson, et al.
Human Genetics|April 5, 2003
A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21Simeon A Boyadjiev, Cristina M Justice, Wafaa Eyaid, et al.
Human Heredity|November 17, 2012
Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2Nancy H Miller, Cristina M Justice, Beth Marosy, et al.
Human Genetics|June 22, 2026
Combined family-based association and linkage analyses in families affected by attention-deficit hyperactivity disorderCristina M Justice, Kwangmi Ahn, Benjamin Jung, et al.
Human Heredity|October 16, 2010
Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired familiesTabatha R Simmons, Judy F Flax, Marco A Azaro, et al.
Genes|May 28, 2022
Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic CraniosynostosisCristina M Justice, Anthony M Musolf, Araceli Cuellar, et al.
Pageof 26

Showing results (221-230 of 254) with videos related to

Sort By:
Pageof 26
Genes|September 23, 2022
<i>TBX3</i> and <i>EFNA4</i> Variant in a Family with Ulnar-Mammary Syndrome and Sagittal CraniosynostosisMoon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, et al.
BMC Proceedings|March 1, 2012
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence dataClaire L Simpson, Cristina M Justice, Mera Krishnan, et al.
International Forum of Allergy & Rhinology|April 11, 2025
Silastic Septal Splints in the Management of Refractory Epistaxis in Hereditary Hemorrhagic TelangiectasiaAvraham Adelman, Eunice Im, Brett Labella, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32Nancy H Miller, Beth Marosy, Cristina M Justice, et al.
Blood Vessels, Thrombosis & Hemostasis|October 16, 2025
Nasal RADA16 hydrogel application decreases epistaxis severity scores in adults with hereditary hemorrhagic telangiectasiaAvraham Adelman, Eunice Im, Lindsey Jackson, et al.
Human Genetics|April 5, 2003
A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21Simeon A Boyadjiev, Cristina M Justice, Wafaa Eyaid, et al.
Human Heredity|November 17, 2012
Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2Nancy H Miller, Cristina M Justice, Beth Marosy, et al.
Human Genetics|June 22, 2026
Combined family-based association and linkage analyses in families affected by attention-deficit hyperactivity disorderCristina M Justice, Kwangmi Ahn, Benjamin Jung, et al.
Human Heredity|October 16, 2010
Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired familiesTabatha R Simmons, Judy F Flax, Marco A Azaro, et al.
Genes|May 28, 2022
Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic CraniosynostosisCristina M Justice, Anthony M Musolf, Araceli Cuellar, et al.
Pageof 26