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Wilfredo Torres-Martinez

Showing results (1-10 of 25) with videos related to

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American Journal of Medical Genetics. Part A|January 30, 2007
Two cases further delineating the Sakoda complexMelissa A Dempsey, Wilfredo Torres-Martinez, Laurence E Walsh
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 24, 2005
Johnson-McMillin syndrome: report of a new case with novel featuresLisa J Cushman, Wilfredo Torres-Martinez, David D Weaver
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 3, 2010
Spurious case of XX maleness in a patient with a history of Wiskott-Aldrich syndromeTodd D Nebesio, Wilfredo Torres-Martinez, Richard C Rink, et al.
Cytogenetic and Genome Research|December 14, 2022
Genotype-Phenotype Correlation of Distal 2q37 DeletionsAiko Iwata-Otsubo, Kahlen R Darr, Wilfredo Torres-Martinez, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Association of a p.Pro786Leu variant in COL2A1 with mild spondyloepiphyseal dysplasia congenita in a three-generation familyPaul R Mark, Wilfredo Torres-Martinez, Ralph S Lachman, et al.
Journal of Genetic Counseling|October 3, 2020
Positive and negative professionalism experiences of genetic counseling students in the United States and CanadaPauline Aamodt, Leah Wetherill, Paula Delk, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
On the spectrum of limb-body wall complex, exstrophy of the cloaca, and urorectal septum malformation sequenceCristin A Heyroth-Griffis, David D Weaver, Philip Faught, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
Prenatal diagnosis of Carpenter syndrome: looking beyond craniosynostosis and polysyndactylyAnna S Victorine, Jennifer Weida, Karrie A Hines, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Rubinstein-Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: a contiguous gene syndrome?Cezary Wójcik, Kim Volz, Maria Ranola, et al.
American Journal of Medical Genetics. Part A|August 1, 2007
A case of de novo partial tetrasomy of distal 6p and review of the literatureRyan Stohler, Ellen Kucharski, Emily Farrow, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|January 30, 2007
Two cases further delineating the Sakoda complexMelissa A Dempsey, Wilfredo Torres-Martinez, Laurence E Walsh
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 24, 2005
Johnson-McMillin syndrome: report of a new case with novel featuresLisa J Cushman, Wilfredo Torres-Martinez, David D Weaver
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 3, 2010
Spurious case of XX maleness in a patient with a history of Wiskott-Aldrich syndromeTodd D Nebesio, Wilfredo Torres-Martinez, Richard C Rink, et al.
Cytogenetic and Genome Research|December 14, 2022
Genotype-Phenotype Correlation of Distal 2q37 DeletionsAiko Iwata-Otsubo, Kahlen R Darr, Wilfredo Torres-Martinez, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Association of a p.Pro786Leu variant in COL2A1 with mild spondyloepiphyseal dysplasia congenita in a three-generation familyPaul R Mark, Wilfredo Torres-Martinez, Ralph S Lachman, et al.
Journal of Genetic Counseling|October 3, 2020
Positive and negative professionalism experiences of genetic counseling students in the United States and CanadaPauline Aamodt, Leah Wetherill, Paula Delk, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
On the spectrum of limb-body wall complex, exstrophy of the cloaca, and urorectal septum malformation sequenceCristin A Heyroth-Griffis, David D Weaver, Philip Faught, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
Prenatal diagnosis of Carpenter syndrome: looking beyond craniosynostosis and polysyndactylyAnna S Victorine, Jennifer Weida, Karrie A Hines, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Rubinstein-Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: a contiguous gene syndrome?Cezary Wójcik, Kim Volz, Maria Ranola, et al.
American Journal of Medical Genetics. Part A|August 1, 2007
A case of de novo partial tetrasomy of distal 6p and review of the literatureRyan Stohler, Ellen Kucharski, Emily Farrow, et al.
Pageof 3