Search research articles
Contact Us
Filters
Showing results (1-10 of 24) with videos related to
Page
of 3
Sort By:
Clinical Dysmorphology
|
October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literature
Anne M Slavotinek, Felicitas Lacbawan
Seminars in Arthritis and Rheumatism
|
December 2, 2015
Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinic
Qingping Yao, Felicitas Lacbawan, Jianbo Li
Clinical Dysmorphology
|
October 18, 2003
A female infant with duplication of chromosome 2q33 to 2q37.3
Anne 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 syndrome
Anne M Slavotinek, Elizabeth Dubovsky, Harry C Dietz, et al.
Rheumatology (Oxford, England)
|
June 14, 2015
NOD2-associated autoinflammatory disease: a large cohort study
Qingping 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 humans
Erich 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 family
Benjamin 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-Analysis
Matthew Rubinstein, Robert Hirsch, Kakali Bandyopadhyay, et al.
Pharmacogenomics
|
May 7, 2014
Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based care
Kathryn Teng, Jennifer DiPiero, Thad Meese, et al.
Human Molecular Genetics
|
September 16, 2008
Mutations in the human SIX3 gene in holoprosencephaly are loss of function
Sabina Domené, Erich Roessler, Kenia B El-Jaick, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Clinical Dysmorphology
|
October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literature
Anne M Slavotinek, Felicitas Lacbawan
Seminars in Arthritis and Rheumatism
|
December 2, 2015
Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinic
Qingping Yao, Felicitas Lacbawan, Jianbo Li
Clinical Dysmorphology
|
October 18, 2003
A female infant with duplication of chromosome 2q33 to 2q37.3
Anne 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 syndrome
Anne M Slavotinek, Elizabeth Dubovsky, Harry C Dietz, et al.
Rheumatology (Oxford, England)
|
June 14, 2015
NOD2-associated autoinflammatory disease: a large cohort study
Qingping 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 humans
Erich 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 family
Benjamin 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-Analysis
Matthew Rubinstein, Robert Hirsch, Kakali Bandyopadhyay, et al.
Pharmacogenomics
|
May 7, 2014
Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based care
Kathryn Teng, Jennifer DiPiero, Thad Meese, et al.
Human Molecular Genetics
|
September 16, 2008
Mutations in the human SIX3 gene in holoprosencephaly are loss of function
Sabina Domené, Erich Roessler, Kenia B El-Jaick, et al.
Page
of 3