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Felicitas Lacbawan

Showing results (1-10 of 24) with videos related to

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Clinical Dysmorphology|October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literatureAnne M Slavotinek, Felicitas Lacbawan
Seminars in Arthritis and Rheumatism|December 2, 2015
Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinicQingping Yao, Felicitas Lacbawan, Jianbo Li
Clinical Dysmorphology|October 18, 2003
A female infant with duplication of chromosome 2q33 to 2q37.3Anne M Slavotinek, Debra Boles, Felicitas Lacbawan
American Journal of Medical Genetics|July 13, 2002
Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndromeAnne M Slavotinek, Elizabeth Dubovsky, Harry C Dietz, et al.
Rheumatology (Oxford, England)|June 14, 2015
NOD2-associated autoinflammatory disease: a large cohort studyQingping Yao, Min Shen, Christine McDonald, et al.
Human Genetics|February 3, 2009
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humansErich Roessler, Yong Ma, Maia V Ouspenskaia, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
A novel SIX3 mutation segregates with holoprosencephaly in a large familyBenjamin D Solomon, Felicitas Lacbawan, Mahim Jain, et al.
American Journal of Clinical Pathology|February 23, 2018
Effectiveness of Practices to Support Appropriate Laboratory Test Utilization: A Laboratory Medicine Best Practices Systematic Review and Meta-AnalysisMatthew Rubinstein, Robert Hirsch, Kakali Bandyopadhyay, et al.
Pharmacogenomics|May 7, 2014
Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based careKathryn Teng, Jennifer DiPiero, Thad Meese, et al.
Human Molecular Genetics|September 16, 2008
Mutations in the human SIX3 gene in holoprosencephaly are loss of functionSabina Domené, Erich Roessler, Kenia B El-Jaick, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Clinical Dysmorphology|October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literatureAnne M Slavotinek, Felicitas Lacbawan
Seminars in Arthritis and Rheumatism|December 2, 2015
Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinicQingping Yao, Felicitas Lacbawan, Jianbo Li
Clinical Dysmorphology|October 18, 2003
A female infant with duplication of chromosome 2q33 to 2q37.3Anne M Slavotinek, Debra Boles, Felicitas Lacbawan
American Journal of Medical Genetics|July 13, 2002
Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndromeAnne M Slavotinek, Elizabeth Dubovsky, Harry C Dietz, et al.
Rheumatology (Oxford, England)|June 14, 2015
NOD2-associated autoinflammatory disease: a large cohort studyQingping Yao, Min Shen, Christine McDonald, et al.
Human Genetics|February 3, 2009
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humansErich Roessler, Yong Ma, Maia V Ouspenskaia, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
A novel SIX3 mutation segregates with holoprosencephaly in a large familyBenjamin D Solomon, Felicitas Lacbawan, Mahim Jain, et al.
American Journal of Clinical Pathology|February 23, 2018
Effectiveness of Practices to Support Appropriate Laboratory Test Utilization: A Laboratory Medicine Best Practices Systematic Review and Meta-AnalysisMatthew Rubinstein, Robert Hirsch, Kakali Bandyopadhyay, et al.
Pharmacogenomics|May 7, 2014
Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based careKathryn Teng, Jennifer DiPiero, Thad Meese, et al.
Human Molecular Genetics|September 16, 2008
Mutations in the human SIX3 gene in holoprosencephaly are loss of functionSabina Domené, Erich Roessler, Kenia B El-Jaick, et al.
Pageof 3