A Toolkit for Genetics Providers in Follow‐up of Patients with Non‐diagnostic Exome Sequencing
Diane B. Zastrow,Jennefer N. Kohler,Devon Bonner,Chloe M. Reuter,Liliana Fernandez,Megan E. Grove,Dianna G. Fisk,Yaping Yang,Christine M. Eng,Patricia A. Ward,David Bick,Elizabeth A. Worthey,Paul G. Fisher,Euan A. Ashley,Jonathan A. Bernstein,Matthew T. Wheeler,David R. Adams,Aaron Aday, Mercedes E. Alejandro,Patrick Allard,Mahshid S. Azamian,Carlos A. Bacino,Eva Baker,Ashok Balasubramanyam,Hayk Barseghyan,Gabriel F. Batzli,Alan H. Beggs,Babak Behnam,Hugo J. Bellen,Anna Bican,David P. Bick,Camille L. Birch,Braden E. Boone,Bret L. Bostwick,Lauren C. Briere,Elly Brokamp,Donna M. Brown,Matthew Brush,Elizabeth A. Burke,Lindsay C. Burrage,Manish J. Butte,Shan Chen,Gary D. Clark,Terra R. Coakley,Joy D. Cogan,Heather A. Colley,Cynthia M. Cooper,Heidi Cope,William J. Craigen,Precilla D'Souza,Mariska Davids,Jyoti G. Dayal,Esteban C. Dell'Angelica,Shweta U. Dhar,Katrina M. Dipple, Laurel A. Donnell-Fink,Naghmeh Dorrani,Daniel C. Dorset,Emilie D. Douine,David D. Draper,Annika M. Dries,David J. Eckstein,Lisa T. Emrick,Gregory M. Enns,Ascia Eskin,Cecilia Esteves,Tyra Estwick,Laura Fairbrother,Carlos Ferreira,Elizabeth L. Fieg,Brent L. Fogel,William A. Gahl,Emily Glanton,Rena A. Godfrey,Alica M. Goldman,David B. Goldstein,Sarah E. Gould,Jean-Philippe F. Gourdine,Catherine A. Groden,Andrea L. Gropman,Melissa Haendel,Rizwan Hamid,Neil A. Hanchard,Francis High,Ingrid A. Holm,Jason Hom,Ellen M. Howerton, Yong Huang,Fariha Jamal,Yong-hui Jiang,Jean M. Johnston,Angela L. Jones,Lefkothea Karaviti,David M. Koeller,Isaac S. Kohane,Donna M. Krasnewich,Susan Korrick,Mary Koziura,Joel B. Krier,Jennifer E. Kyle,Seema R. Lalani,C. Christopher Lau,Jozef Lazar,Kimberly LeBlanc,Brendan H. Lee,Hane Lee,Shawn E. Levy,Richard A. Lewis,Sharyn A. Lincoln,Sandra K. Loo,Joseph Loscalzo,Richard L. Maas,Ellen F. Macnamara,Calum A. MacRae,Valerie V. Maduro,Marta M. Majcherska,May Christine V. Malicdan,Laura A. Mamounas,Teri A. Manolio,Thomas C. Markello,Ronit Marom, Martin,Julian A. Martinez-Agosto,Shruti Marwaha,Thomas May,Allyn McConkie-Rosell,Colleen E. McCormack,Alexa T. McCray,Jason D. Merker,Thomas O. Metz,Matthew Might,Paolo M. Moretti,Marie Morimoto,Michele E. Nehrebecky,Stan F. Nelson,J. Scott Newberry,John H. Newman,Sarah K. Nicholas,Donna Novacic,Jordan S. Orange,James P. Orengo,J. Carl Pallais,Christina G. S. Palmer,Jeanette C. Papp,John H. Postlethwait,Lorraine Potocki,Barbara N. Pusey,Lynette Rives,Amy K. Robertson,Lance H. Rodan,Jill A. Rosenfeld,Jacinda B. Sampson,Susan L. Samson,Kelly Schoch,Daryl A. Scott,Lisa Shakachite,Prashant Sharma,Vandana Shashi,Rebecca Signer,Edwin K. Silverman,Janet S. Sinsheimer,Kevin S. Smith,Rebecca C. Spillmann,Joan M. Stoler,Nicholas Stong,Jennifer A. Sullivan,David A. Sweetser,Queenie K. -G. Tan,Cynthia J. Tifft,Camilo Toro,Alyssa A. Tran,Tiina K. Urv,Eric Vilain,Tiphanie P. Vogel,Daryl M. Waggott,Colleen E. Wahl,Nicole M. Walley,Chris A. Walsh,Melissa Walker,Jijun Wan,Michael F. Wangler,Katrina M. Waters,Bobbie-Jo M. Webb-Robertson,Monte Westerfield,Anastasia L. Wise,Lynne A. Wolfe,Shinya Yamamoto,John Yang,Amanda J. Yoon,Guoyun Yu,Chunli Zhao,Allison Zheng
Journal of Genetic Counseling（2019）
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关键词
exome sequencing,genome sequencing,rare diseases,sequencing reanalysis,undiagnosed diseases
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