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B Irons

Showing results (91-100 of 101) with videos related to

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Fetal Diagnosis and Therapy|June 12, 1999
Antenatal therapy of Smith-Lemli-Opitz syndromeM B Irons, J Nores, T L Stewart, et al.
Plos One|March 28, 2014
Foraging responses of black-legged kittiwakes to prolonged food-shortages around colonies on the Bering Sea shelfRosana Paredes, Rachael A Orben, Robert M Suryan, et al.
American Journal of Medical Genetics. Part A|March 29, 2025
Expanding the SIAH1-Associated Phenotypic Spectrum: Insights From Loss-of-Function VariantsLiza Douiev, Paula Fernandez Alvarez, Marika Frank, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) geneHagit Baris, Bassem A Bejjani, Wen-Hann Tan, et al.
Prenatal Diagnosis|July 13, 2006
Identifying Smith-Lemli-Opitz syndrome in conjunction with prenatal screening for Down syndromeWendy Y Craig, James E Haddow, Glenn E Palomaki, et al.
Global Change Biology|August 2, 2019
Diverging phenological responses of Arctic seabirds to an earlier springSébastien Descamps, Francisco Ramírez, Sigurd Benjaminsen, et al.
American Journal of Human Genetics|February 24, 2009
Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasiaDeborah Krakow, Joris Vriens, Natalia Camacho, et al.
Virology Journal|June 6, 2008
Prevalence of Influenza A viruses in wild migratory birds in Alaska: patterns of variation in detection at a crossroads of intercontinental flywaysHon S Ip, Paul L Flint, J Christian Franson, et al.
Global Change Biology|April 8, 2017
Circumpolar dynamics of a marine top-predator track ocean warming ratesSébastien Descamps, Tycho Anker-Nilssen, Robert T Barrett, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Fetal Diagnosis and Therapy|June 12, 1999
Antenatal therapy of Smith-Lemli-Opitz syndromeM B Irons, J Nores, T L Stewart, et al.
Plos One|March 28, 2014
Foraging responses of black-legged kittiwakes to prolonged food-shortages around colonies on the Bering Sea shelfRosana Paredes, Rachael A Orben, Robert M Suryan, et al.
American Journal of Medical Genetics. Part A|March 29, 2025
Expanding the SIAH1-Associated Phenotypic Spectrum: Insights From Loss-of-Function VariantsLiza Douiev, Paula Fernandez Alvarez, Marika Frank, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) geneHagit Baris, Bassem A Bejjani, Wen-Hann Tan, et al.
Prenatal Diagnosis|July 13, 2006
Identifying Smith-Lemli-Opitz syndrome in conjunction with prenatal screening for Down syndromeWendy Y Craig, James E Haddow, Glenn E Palomaki, et al.
Global Change Biology|August 2, 2019
Diverging phenological responses of Arctic seabirds to an earlier springSébastien Descamps, Francisco Ramírez, Sigurd Benjaminsen, et al.
American Journal of Human Genetics|February 24, 2009
Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasiaDeborah Krakow, Joris Vriens, Natalia Camacho, et al.
Virology Journal|June 6, 2008
Prevalence of Influenza A viruses in wild migratory birds in Alaska: patterns of variation in detection at a crossroads of intercontinental flywaysHon S Ip, Paul L Flint, J Christian Franson, et al.
Global Change Biology|April 8, 2017
Circumpolar dynamics of a marine top-predator track ocean warming ratesSébastien Descamps, Tycho Anker-Nilssen, Robert T Barrett, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, et al.
Pageof 11