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Amihood Singer

Showing results (41-50 of 55) with videos related to

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Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
Archives of Gynecology and Obstetrics|August 8, 2020
Chromosomal microarray should be performed for cases of fetal short long bones detected prenatallyKeren Tzadikevitch Geffen, Amihood Singer, Idit Maya, et al.
Human Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.
Obstetrics and Gynecology|November 7, 2018
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic AnomaliesLena Sagi-Dain, Idit Maya, Adi Reches, et al.
American Journal of Medical Genetics. Part A|November 15, 2017
Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patientsDaphné Lehalle, Umut Altunoglu, Ange-Line Bruel, et al.
Frontiers in Pediatrics|April 18, 2022
Refining the Phenotypic Spectrum of <i>KMT5B</i>-Associated Developmental DelayAviva Eliyahu, Ortal Barel, Lior Greenbaum, et al.
Science Translational Medicine|September 10, 2020
Characterization of <i>ANGPT2</i> mutations associated with primary lymphedemaVeli-Matti Leppänen, Pascal Brouillard, Emilia A Korhonen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 18, 2023
The new face of cystic fibrosis in the era of population genetic carrier screeningMiri Dotan, Hannah Blau, Amihood Singer, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screeningDoron M Behar, Ori Inbar, Michal Shteinberg, et al.
American Journal of Human Genetics|January 31, 2012
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathyPia Ostergaard, Michael A Simpson, Antonella Mendola, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
Archives of Gynecology and Obstetrics|August 8, 2020
Chromosomal microarray should be performed for cases of fetal short long bones detected prenatallyKeren Tzadikevitch Geffen, Amihood Singer, Idit Maya, et al.
Human Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.
Obstetrics and Gynecology|November 7, 2018
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic AnomaliesLena Sagi-Dain, Idit Maya, Adi Reches, et al.
American Journal of Medical Genetics. Part A|November 15, 2017
Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patientsDaphné Lehalle, Umut Altunoglu, Ange-Line Bruel, et al.
Frontiers in Pediatrics|April 18, 2022
Refining the Phenotypic Spectrum of <i>KMT5B</i>-Associated Developmental DelayAviva Eliyahu, Ortal Barel, Lior Greenbaum, et al.
Science Translational Medicine|September 10, 2020
Characterization of <i>ANGPT2</i> mutations associated with primary lymphedemaVeli-Matti Leppänen, Pascal Brouillard, Emilia A Korhonen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 18, 2023
The new face of cystic fibrosis in the era of population genetic carrier screeningMiri Dotan, Hannah Blau, Amihood Singer, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screeningDoron M Behar, Ori Inbar, Michal Shteinberg, et al.
American Journal of Human Genetics|January 31, 2012
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathyPia Ostergaard, Michael A Simpson, Antonella Mendola, et al.
Pageof 6