المؤلفون: Joseph, Jenica (ORCID 0000-0002-4682-6612), Shilling, Tammy (ORCID 0000-0001-8775-7724), Ferguson, Heather L. (ORCID 0000-0003-2056-2695), Kijai, Jimmy (ORCID 0000-0002-5224-7027)

المصدر: Journal of Research on Christian Education. 2023 32(1-2):65-83.

Peer Reviewed: Y

Page Count: 19

Descriptors: Speech Language Pathology, Allied Health Personnel, Clinical Experience, Simulation, Learning Experience, Formative Evaluation

المؤلفون: Redin, Claire, Brand, Harrison, Collins, Ryan L., Kammin, Tammy, Mitchell, Elyse, Hodge, Jennelle C., Hanscom, Carrie, Pillalamarri, Vamsee, Seabra, Catarina M., Abbott, Mary-Alice, Abdul-Rahman, Omar A., Aberg, Erika, Adley, Rhett, Alcaraz-Estrada, Sofia L., Alkuraya, Fowzan S., An, Yu, Anderson, Mary-Anne, Antolik, Caroline, Anyane-Yeboa, Kwame, Atkin, Joan F., Bartell, Tina, Bernstein, Jonathan A., Beyer, Elizabeth, Blumenthal, Ian, Bongers, Ernie M. H. F., Brilstra, Eva H., Brown, Chester W., Bruggenwirth, Hennie T., Callewaert, Bert, Chiang, Colby, Corning, Ken, Cox, Helen, Cuppen, Edwin, Currall, Benjamin B., Cushing, Tom, David, Dezso, Deardorff, Matthew A., Dheedene, Annelies, D'Hooghe, Marc, de Vries, Bert B. A., Earl, Dawn L., Ferguson, Heather L., Fisher, Heather, FitzPatrick, David R., Gerrol, Pamela, Giachino, Daniela, Glessner, Joseph T., Gliem, Troy, Grady, Margo, Graham, Brett H., Griffis, Cristin, Gripp, Karen W., Gropman, Andrea L., Hanson-Kahn, Andrea, Harris, David J., Hayden, Mark A., Hill, Rosamund, Hochstenbach, Ron, Hoffman, Jodi D., Hopkin, Robert J., Hubshman, Monika W., Innes, A. Micheil, Irons, Mira, Irving, Melita, Jacobsen, Jessie C., Janssens, Sandra, Jewett, Tamison, Johnson, John P., Jongmans, Marjolijn C., Kahler, Stephen G., Koolen, David A., Korzelius, Jerome, Kroisel, Peter M., Lacassie, Yves, Lawless, William, Lemyre, Emmanuelle, Leppig, Kathleen, Levin, Alex V., Li, Haibo, Li, Hong, Liao, Eric C., Lim, Cynthia, Lose, Edward J., Lucente, Diane, Macera, Michael J., Manavalan, Poornima, Mandrile, Giorgia, Marcelis, Carlo L., Margolin, Lauren, Mason, Tamara, Masser-Frye, Diane, McClellan, Michael W., Mendoza, Cinthya J. Zepeda, Menten, Bjorn, Middelkamp, Sjors, Mikami, Liya R., Moe, Emily, Mohammed, Shehla, Mononen, Tarja, Mortenson, Megan E., Moya, Graciela, Nieuwint, Aggie W., Ordulu, Zehra, Parkash, Sandhya, Pauker, Susan P., Pereira, Shahrin, Perrin, Danielle, Phelan, Katy, Pina Aguilar, Raul E., Poddighe, Pino J., Pregno, Giulia, Raskin, Salmo, Reis, Linda, Rhead, William, Rita, Debra, Renkens, Ivo, Roelens, Filip, Ruliera, Jayla, Rump, Patrick, Schilit, Samantha L. P., Shaheen, Ranad, Sparkes, Rebecca, Spiegel, Erica, Stevens, Blair, Stone, Matthew R., Tagoe, Julia, Thakuria, Joseph V., van Bon, Bregje W., van de Kamp, Jiddeke, van Der Burgt, Ineke, van Essen, Ton, van Ravenswaaij-Arts, Conny M., van Roosmalen, Markus J., Vergult, Sarah, Volker-Touw, Catharina M. L., Warburton, Dorothy P., Waterman, Matthew J., Wiley, Susan, Wilson, Anna, Yerena-de Vega, Maria de la Concepcion A., Zori, Roberto T., Levy, Brynn, Brunner, Han G., de Leeuw, Nicole, Kloosterman, Wigard P., Thorland, Erik C., Morton, Cynthia C., Gusella, James F., Talkowski, Michael E.

المصدر: Redin , C , Brand , H , Collins , R L , Kammin , T , Mitchell , E , Hodge , J C , Hanscom , C , Pillalamarri , V , Seabra , C M , Abbott , M-A , Abdul-Rahman , O A , Aberg , E , Adley , R , Alcaraz-Estrada , S L , Alkuraya , F S , An , Y , Anderson , M-A , Antolik , C , Anyane-Yeboa , K , Atkin , J F , Bartell , T , Bernstein , J A , Beyer , E ....

مصطلحات موضوعية: AUTISM SPECTRUM DISORDER, DE-NOVO MUTATIONS, SEVERE MENTAL-RETARDATION, OF-FUNCTION MUTATIONS, MICRODELETION SYNDROME, CHROMOSOME REARRANGEMENTS, INTELLECTUAL DISABILITY, STRUCTURAL VARIATION, DEVELOPMENTAL DELAY, CANCER GENOMES

الاتاحة: https://hdl.handle.net/11370/2cc769f3-7d83-4416-86f5-f75f2161ded9
https://research.rug.nl/en/publications/2cc769f3-7d83-4416-86f5-f75f2161ded9
https://doi.org/10.1038/ng.3720
http://europepmc.org/articles/pmc5307971?pdf=render

المؤلفون: Higgins, Anne W., Alkuraya, Fowzan S., Bosco, Amy F., Brown, Kerry K., Bruns, Gail A.P., Donovan, Diana J., Eisenman, Robert, Fan, Yanli, Farra, Chantal G., Ferguson, Heather L., Gusella, James F., Harris, David J., Herrick, Steven R., Kelly, Chantal, Kim, Hyung-Goo, Kishikawa, Shotaro, Korf, Bruce R., Kulkarni, Shashikant, Lally, Eric, Leach, Natalia T., Lemyre, Emma, Lewis, Janine, Ligon, Azra H., Lu, Weining, Maas, Richard L., MacDonald, Marcy E., Moore, Steven D.P., Peters, Roxanna E., Quade, Bradley J., Quintero-Rivera, Fabiola, Saadi, Irfan, Shen, Yiping, Shendure, Jay, Williamson, Robin E., Morton, Cynthia C.

المصدر: The American Journal of Human Genetics ; volume 82, issue 3, page 712-722 ; ISSN 0002-9297

الاتاحة: http://dx.doi.org/10.1016/j.ajhg.2008.01.011
https://api.elsevier.com/content/article/PII:S0002929708001596?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929708001596?httpAccept=text/plain

المؤلفون: Ligon, Azra H., Moore, Steven D.P., Parisi, Melissa A., Mealiffe, Matthew E., Harris, David J., Ferguson, Heather L., Quade, Bradley J., Morton, Cynthia C.

المصدر: The American Journal of Human Genetics ; volume 76, issue 2, page 340-348 ; ISSN 0002-9297

الاتاحة: http://dx.doi.org/10.1086/427565
https://api.elsevier.com/content/article/PII:S0002929707625853?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929707625853?httpAccept=text/plain

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 25-65 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0002

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 196-232 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0006

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 153-195 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0005

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 66-105 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0003

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 106-150 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0004

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 277-288 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0008

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 235-276 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0007

المؤلفون: Ferguson, Heather L.

المصدر: The Proper Order of Things ; page 1-22 ; ISBN 9781503603561 9781503605534

الاتاحة: http://dx.doi.org/10.11126/stanford/9781503603561.003.0001

المؤلفون: FERGUSON, HEATHER L.

المصدر: ISBN 9781503605534 1503605531.

الاتاحة: http://dx.doi.org/10.2307/j.ctvqsdx7n

المؤلفون: Blessing, Patricia, Ferguson, Heather L., Kilinç, Kivanç

المصدر: International Journal of Islamic Architecture; January 2021, Vol. 10 Issue: 1 p11-15, 5p

المؤلفون: Genetica Klinische Genetica, Brain, CMM, Circulatory Health, Cancer, Child Health, Genetica Sectie Genoomdiagnostiek, CMM Groep Cuppen, Genetica, CMM Groep Kloosterman, Redin, Claire, Brand, Harrison, Collins, Ryan L, Kammin, Tammy, Mitchell, Elyse, Hodge, Jennelle C, Hanscom, Carrie, Pillalamarri, Vamsee, Seabra, Catarina M, Abbott, Mary-Alice, Abdul-Rahman, Omar A, Aberg, Erika, Adley, Rhett, Alcaraz-Estrada, Sofia L, Alkuraya, Fowzan S, An, Yu, Anderson, Mary-Anne, Antolik, Caroline, Anyane-Yeboa, Kwame, Atkin, Joan F, Bartell, Tina, Bernstein, Jonathan A, Beyer, Elizabeth, Blumenthal, Ian, Bongers, Ernie M H F, Brilstra, Eva H, Brown, Chester W, Brüggenwirth, Hennie T, Callewaert, Bert, Chiang, Colby, Corning, Ken, Cox, Helen, Cuppen, Edwin, Currall, Benjamin B, Cushing, Tom, David, Dezso, Deardorff, Matthew A, Dheedene, Annelies, D'Hooghe, Marc, de Vries, Bert B A, Earl, Dawn L, Ferguson, Heather L, Fisher, Heather, FitzPatrick, David R, Gerrol, Pamela, Giachino, Daniela, Glessner, Joseph T, Gliem, Troy, Grady, Margo, Graham, Brett H, Griffis, Cristin, Gripp, Karen W, Gropman, Andrea L, Hanson-Kahn, Andrea, Harris, David J, Hayden, Mark A, Hill, Rosamund, Hochstenbach, Ron, Hoffman, Jodi D, Hopkin, Robert J, Hubshman, Monika W, Innes, A Micheil, Irons, Mira, Irving, Melita, Jacobsen, Jessie C, Janssens, Sandra, Jewett, Tamison, Johnson, John P, Jongmans, Marjolijn C, Kahler, Stephen G, Koolen, David A, Korzelius, Jerome, Kroisel, Peter M, Lacassie, Yves, Lawless, William, Lemyre, Emmanuelle, Leppig, Kathleen, Levin, Alex V, Li, Haibo, Li, Hong, Liao, Eric C, Lim, Cynthia, Lose, Edward J, Lucente, Diane, Macera, Michael J, Manavalan, Poornima, Mandrile, Giorgia, Marcelis, Carlo L, Margolin, Lauren, Mason, Tamara, Masser-Frye, Diane, McClellan, Michael W, Mendoza, Cinthya J Zepeda, Menten, Björn, Middelkamp, Sjors, Mikami, Liya R, Moe, Emily, Mohammed, Shehla, Mononen, Tarja, Mortenson, Megan E, Moya, Graciela, Nieuwint, Aggie W, Ordulu, Zehra, Parkash, Sandhya, Pauker, Susan P, Pereira, Shahrin, Perrin, Danielle, Phelan, Katy, Aguilar, Raul E Piña, Poddighe, Pino J, Pregno, Giulia, Raskin, Salmo, Reis, Linda, Rhead, William, Rita, Debra, Renkens, Ivo, Roelens, Filip, Ruliera, Jayla, Rump, Patrick, Schilit, Samantha L P, Shaheen, Ranad, Sparkes, Rebecca, Spiegel, Erica, Stevens, Blair, Stone, Matthew R, Tagoe, Julia, Thakuria, Joseph V, van Bon, Bregje W, van de Kamp, Jiddeke, van Der Burgt, Ineke, van Essen, Ton, van Ravenswaaij-Arts, Conny M, van Roosmalen, Markus J, Vergult, Sarah, Volker-Touw, Catharina M L, Warburton, Dorothy P, Waterman, Matthew J, Wiley, Susan, Wilson, Anna, Yerena-de Vega, Maria de la Concepcion A, Zori, Roberto T, Levy, Brynn, Brunner, Han G, de Leeuw, Nicole, Kloosterman, Wigard P, Thorland, Erik C, Morton, Cynthia C, Gusella, James F, Talkowski, Michael E

URL: https://doi.org/10.1038/ng.3720
http://hdl.handle.net/1874/343058
https://dspace.library.uu.nl/handle/1874/343058
1061-4036
Nature Genetics
49
1

المؤلفون: Brown, Kerry K, Reiss, Jacob A, Crow, Kate, Ferguson, Heather L, Kelly, Chantal, Fritzsch, Bernd, Morton, Cynthia C

المصدر: Brown , K K , Reiss , J A , Crow , K , Ferguson , H L , Kelly , C , Fritzsch , B & Morton , C C 2010 , ' Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35). ' , Human Genetics , vol. 127 , no. 1 . https://doi.org/10.1007/s00439-009-0736-4

Relation: https://research.manchester.ac.uk/en/publications/be0e2ba9-ba45-4e8f-8fde-9930680953d4

الاتاحة: https://research.manchester.ac.uk/en/publications/be0e2ba9-ba45-4e8f-8fde-9930680953d4
https://doi.org/10.1007/s00439-009-0736-4

المؤلفون: Brown, Kerry K, PhD, Reiss, Jacob A, Crow, Kate, Ferguson, Heather L, Kelly, Chantal, Fritzsch, Bernd, Morton, Cynthia C

المصدر: Department of Pathology & Laboratory Medicine

مصطلحات موضوعية: Abnormalities, Multiple, Adolescent, Adult, Animals, Base Sequence, Child, Preschool, Chromosome Inversion, Chromosomes, Human, Pair 7, Craniofacial Abnormalities, Embryo, Mammalian, Enhancer Elements, Genetic, Family Health, Female, Gene Transfer Techniques, Hearing Loss, Homeodomain Proteins, Humans, In Situ Hybridization, Fluorescence, Male, Mice, Middle Aged, Pedigree, Sequence Deletion

Relation: https://scholarlyworks.lvhn.org/pathology-laboratory-medicine/677; https://pubmed.ncbi.nlm.nih.gov/19707792/

الاتاحة: https://scholarlyworks.lvhn.org/pathology-laboratory-medicine/677
https://pubmed.ncbi.nlm.nih.gov/19707792/

المؤلفون: Higgins, Anne W, Alkuraya, Fowzan S, Bosco, Amy F, Brown, Kerry K, PhD, Bruns, Gail A P, Donovan, Diana J, Eisenman, Robert, Fan, Yanli, Farra, Chantal G, Ferguson, Heather L, Gusella, James F, Harris, David J, Herrick, Steven R, Kelly, Chantal, Kim, Hyung-Goo, Kishikawa, Shotaro, Korf, Bruce R, Kulkarni, Shashikant, Lally, Eric, Leach, Natalia T, Lemyre, Emma, Lewis, Janine, Ligon, Azra H, Lu, Weining, Maas, Richard L, MacDonald, Marcy E, Moore, Steven D P, Peters, Roxanna E, Quade, Bradley J, Quintero-Rivera, Fabiola, Saadi, Irfan, Shen, Yiping, Shendure, Jay, Williamson, Robin E, Morton, Cynthia C

المصدر: Department of Pathology & Laboratory Medicine

مصطلحات موضوعية: Chromosome Breakage, Chromosome Mapping, Congenital Abnormalities, Genome, Human, Human Development, Human Genome Project, Humans, Department of Pathology and Laboratory Medicine, Medicine and Health Sciences

Relation: https://scholarlyworks.lvhn.org/pathology-laboratory-medicine/685; https://pubmed.ncbi.nlm.nih.gov/18319076/

الاتاحة: https://scholarlyworks.lvhn.org/pathology-laboratory-medicine/685
https://pubmed.ncbi.nlm.nih.gov/18319076/

المؤلفون: Deere, Michelle, Sanford, Tiffany, Ferguson, Heather L., Daniels, Karla, Hecht, Jacqueline T.

المصدر: American Journal of Medical Genetics ; volume 80, issue 5, page 510-513 ; ISSN 0148-7299 1096-8628

الاتاحة: http://dx.doi.org/10.1002/(sici)1096-8628(19981228)80:5%3C510::aid-ajmg14%3E3.0.co%3B2-f
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2F(SICI)1096-8628(19981228)80:5%3C510::AID-AJMG14%3E3.0.CO%3B2-F
https://onlinelibrary.wiley.com/doi/full/10.1002/(SICI)1096-8628(19981228)80:5%3C510::AID-AJMG14%3E3.0.CO%3B2-F

المؤلفون: Ferguson, Heather L., Deere, Michelle, Evans, Randall, Rotta, Julie, Hall, Judith G., Hecht, Jacqueline T.

المصدر: American Journal of Medical Genetics ; volume 70, issue 3, page 287-291 ; ISSN 0148-7299 1096-8628

الاتاحة: http://dx.doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C287::aid-ajmg14%3E3.0.co%3B2-h
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2F(SICI)1096-8628(19970613)70:3%3C287::AID-AJMG14%3E3.0.CO%3B2-H
https://onlinelibrary.wiley.com/doi/full/10.1002/(SICI)1096-8628(19970613)70:3%3C287::AID-AJMG14%3E3.0.CO%3B2-H