المؤلفون: Holzinger, Emily R., Li, Qing, Parker, Margaret M., Hetmanski, Jacqueline B., Marazita, Mary L., Mangold, Elisabeth, Ludwig, Kerstin U., Taub, Margaret A., Begum, Ferdouse, Murray, Jeffrey C., Albacha-Hejazi, Hasan, Alqosayer, Khalid, Al-Souki, Giath, Albasha Hejazi, Abdullatiff, Scott, Alan F., Beaty, Terri H., Bailey-Wilson, Joan E.

المساهمون: National Institutes of Health

المصدر: Molecular Genetics & Genomic Medicine ; volume 5, issue 5, page 570-579 ; ISSN 2324-9269

الإتاحة: https://doi.org/10.1002/mgg3.320Test

المؤلفون: Bureau, Alexandre, Begum, Ferdouse, Taub, Margaret A, Hetmanski, Jacqueline B, Parker, Margaret M, Albacha-Hejazi, Hasan, Scott, Alan F, Murray, Jeffrey C, Marazita, Mary L, Bailey-Wilson, Joan E, Beaty, Terri H, Ruczinski, Ingo

المصدر: Genet Epidemiol ; ISSN:1098-2272 ; Volume:43 ; Issue:1

مصطلحات موضوعية: family studies, identity by descent, oral clefts, variant sharing

العلاقة: https://doi.org/10.1002/gepi.22155Test; https://pubmed.ncbi.nlm.nih.gov/30246882Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330140Test/

الإتاحة: https://doi.org/10.1002/gepi.22155Test
https://pubmed.ncbi.nlm.nih.gov/30246882Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330140Test/

المؤلفون: Parker, Margaret M., Lutz, Sharon M., Hobbs, Brian D., Busch, Robert, McDonald, MerryLynn N., Castaldi, Peter J., Beaty, Terri H., Hokanson, John E., Silverman, Edwin K., Cho, Michael H.

المساهمون: National Heart, Lung, and Blood Institute, National Institutes of Health

المصدر: Genetic Epidemiology ; volume 43, issue 3, page 318-329 ; ISSN 0741-0395 1098-2272

الإتاحة: https://doi.org/10.1002/gepi.22192Test

المؤلفون: Bureau, Alexandre, Begum, Ferdouse, Taub, Margaret A., Hetmanski, Jacqueline B., Parker, Margaret M., Albacha‐Hejazi, Hasan, Scott, Alan F., Murray, Jeffrey C., Marazita, Mary L., Bailey‐Wilson, Joan E., Beaty, Terri H., Ruczinski, Ingo

المساهمون: National Institutes of Health

المصدر: Genetic Epidemiology ; volume 43, issue 1, page 37-49 ; ISSN 0741-0395 1098-2272

الإتاحة: https://doi.org/10.1002/gepi.22155Test

المؤلفون: Holzinger, Emily R, Li, Qing, Parker, Margaret M, Hetmanski, Jacqueline B, Marazita, Mary L, Mangold, Elisabeth, Ludwig, Kerstin U, Taub, Margaret A, Begum, Ferdouse, Murray, Jeffrey C, Albacha-Hejazi, Hasan, Alqosayer, Khalid, Al-Souki, Giath, Albasha Hejazi, Abdullatiff, Scott, Alan F, Beaty, Terri H, Bailey-Wilson, Joan E

المصدر: Mol Genet Genomic Med ; ISSN:2324-9269 ; Volume:5 ; Issue:5

مصطلحات موضوعية: DNA sequence data analysis, genetic risk variants, oral clefts, rare variants, statistical genetics

العلاقة: https://doi.org/10.1002/mgg3.320Test; https://pubmed.ncbi.nlm.nih.gov/28944239Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606860Test/

الإتاحة: https://doi.org/10.1002/mgg3.320Test
https://pubmed.ncbi.nlm.nih.gov/28944239Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606860Test/

المؤلفون: Fu, Jack, Beaty, Terri H, Scott, Alan F, Hetmanski, Jacqueline, Parker, Margaret M, Wilson, Joan E Bailey, Marazita, Mary L, Mangold, Elisabeth, Albacha-Hejazi, Hasan, Murray, Jeffrey C, Bureau, Alexandre, Carey, Jacob, Cristiano, Stephen, Ruczinski, Ingo, Scharpf, Robert B

المصدر: Genet Epidemiol ; ISSN:1098-2272 ; Volume:41 ; Issue:1

مصطلحات موضوعية: copy number, multiplex families, oral clefts, rare variants, structural variants

العلاقة: https://doi.org/10.1002/gepi.22010Test; https://pubmed.ncbi.nlm.nih.gov/27910131Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154821Test/

الإتاحة: https://doi.org/10.1002/gepi.22010Test
https://pubmed.ncbi.nlm.nih.gov/27910131Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154821Test/

المؤلفون: Fu, Jack, Beaty, Terri H., Scott, Alan F., Hetmanski, Jacqueline, Parker, Margaret M., Wilson, Joan E. Bailey, Marazita, Mary L., Mangold, Elisabeth, Albacha‐Hejazi, Hasan, Murray, Jeffrey C., Bureau, Alexandre, Carey, Jacob, Cristiano, Stephen, Ruczinski, Ingo, Scharpf, Robert B.

المساهمون: National Human Genome Research Institute, National Institutes of Health

المصدر: Genetic Epidemiology ; volume 41, issue 1, page 61-69 ; ISSN 0741-0395 1098-2272

الإتاحة: https://doi.org/10.1002/gepi.22010Test

المؤلفون: Younkin, Samuel G., Scharpf, Robert B., Schwender, Holger, Parker, Margaret M., Scott, Alan F., Marazita, Mary L., Beaty, Terri H., Ruczinski, Ingo

المساهمون: National Institute of Dental and Craniofacial Research, National Human Genome Research Institute

المصدر: Birth Defects Research Part A: Clinical and Molecular Teratology ; volume 103, issue 4, page 276-283 ; ISSN 1542-0752 1542-0760

الإتاحة: https://doi.org/10.1002/bdra.23362Test

المؤلفون: Begum, Ferdouse, Ruczinski, Ingo, Li, Shengchao, Silverman, Edwin K., Cho, Michael H., Lynch, David A., Curran‐Everett, Douglas, Crapo, James, Scharpf, Robert B., Parker, Margaret M., Hetmanski, Jacqueline B., Beaty, Terri H.

المساهمون: U.S. National Institutes of Health, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Institutes of Health, National Institutes of Health and NIH Roadmap for Medical Research

المصدر: Genetic Epidemiology ; volume 40, issue 1, page 81-88 ; ISSN 0741-0395 1098-2272

الإتاحة: https://doi.org/10.1002/gepi.21943Test

المؤلفون: Parker, Margaret M., Foreman, Marilyn G., Abel, Haley J., Mathias, Rasika A., Hetmanski, Jacqueline B., Crapo, James D., Silverman, Edwin K., Beaty, Terri H.

المساهمون: National Institutes of Health

المصدر: Genetic Epidemiology ; volume 38, issue 7, page 652-659 ; ISSN 0741-0395 1098-2272

الإتاحة: https://doi.org/10.1002/gepi.21847Test