المؤلفون: Au, K. S., Hebert, L., Hillman, P., Baker, C., Brown, M. R., Kim, D.-K., Soldano, K., Garrett, M., Ashley-Koch, A., Lee, S., Gleeson, J., Hixson, J. E., Morrison, A. C., Northrup, H.

المساهمون: Eunice Kennedy Shriver National Institute of Child Health and Human Development

المصدر: Scientific Reports ; volume 11, issue 1 ; ISSN 2045-2322

مصطلحات موضوعية: Multidisciplinary

الإتاحة: https://doi.org/10.1038/s41598-021-83058-7Test
https://www.nature.com/articles/s41598-021-83058-7.pdfTest
https://www.nature.com/articles/s41598-021-83058-7Test

المؤلفون: Kirkpatrick, T J, Au, K-S, Mastrobattista, J M, McCready, M E, Bulman, D E, Northrup, H

مصطلحات موضوعية: Letters to JMG

وصف الملف: text/html

العلاقة: http://jmg.bmj.com/cgi/content/short/40/1/42Test; http://dx.doi.org/10.1136/jmg.40.1.42Test

الإتاحة: https://doi.org/10.1136/jmg.40.1.42Test
http://jmg.bmj.com/cgi/content/short/40/1/42Test

المؤلفون: Peron A., Au K. S., Northrup H.

المساهمون: A. Peron, K.S. Au, H. Northrup

مصطلحات موضوعية: genetic counseling, genetics of TSC, genotype–phenotype correlation, TSC1, TSC2, tuberous sclerosis complex (TSC), Genetic Association Studie, Genetic Testing, Human, Mosaicism, Mutation, Pedigree, Precision Medicine, TOR Serine-Threonine Kinase, Tuberous Sclerosi, Tuberous Sclerosis Complex 1 Protein, Tuberous Sclerosis Complex 2 Protein, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30255984; info:eu-repo/semantics/altIdentifier/wos/WOS:000448788500003; volume:178; issue:3; firstpage:281; lastpage:290; numberofpages:10; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART C, SEMINARS IN MEDICAL GENETICS; http://hdl.handle.net/2434/760064Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85053903775

الإتاحة: https://doi.org/10.1002/ajmg.c.31651Test
http://hdl.handle.net/2434/760064Test

المؤلفون: Au, K. S.

المصدر: IUBMB Life ; volume 39, issue 1, page 197-203 ; ISSN 1521-6543 1521-6551

الإتاحة: https://doi.org/10.1080/15216549600201201Test

المؤلفون: Au, K S, Murrell, J, Buckler, A, Blanton, S H, Northrup, H

المصدر: Journal of Medical Genetics ; volume 33, issue 7, page 559-561 ; ISSN 1468-6244

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1136/jmg.33.7.559Test

المؤلفون: Au, K.‐S., Northrup, H., Kirkpatrick, T.J., Volcik, K.A., Fletcher, J.M., Townsend, I.T., Blanton, S.H., Tyerman, G.H., Villarreal, G., King, T.M.

المصدر: American Journal of Medical Genetics Part A ; volume 139A, issue 3, page 194-198 ; ISSN 1552-4825 1552-4833

الإتاحة: https://doi.org/10.1002/ajmg.a.31002Test

المؤلفون: Priest, J H, Blackston, R D, Au, K S, Ray, S L

مصطلحات موضوعية: Research Article

وصف الملف: text/html

العلاقة: http://jmg.bmj.com/cgi/content/short/12/4/378Test; http://dx.doi.org/10.1136/jmg.12.4.378Test

الإتاحة: https://doi.org/10.1136/jmg.12.4.378Test
http://jmg.bmj.com/cgi/content/short/12/4/378Test

المؤلفون: Au, K S, Chan, W K, Burns, J W, Estes, M K

المصدر: Journal of Virology ; volume 63, issue 11, page 4553-4562 ; ISSN 0022-538X 1098-5514

الإتاحة: https://doi.org/10.1128/jvi.63.11.4553-4562.1989Test

المؤلفون: Yeung, R. T. T., Yeung, D. C. Y., Au, K. S.

المصدر: Cancer (0008543X); Dec1973, Vol. 32 Issue 6, p1482-1489, 8p

المؤلفون: Whitehouse, P. J., Au, K.-S.

المصدر: Advances in Applied Neurological Sciences ; Senile Dementia of the Alzheimer Type ; page 175-182 ; ISSN 0935-0195 ; ISBN 9783642706462 9783642706448

الإتاحة: https://doi.org/10.1007/978-3-642-70644-8_14Test