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Mikhail, Fady
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1

P736: Constitutional mosaic pericentromeric trisomy 8 in a ..:

Gao, Min ; Chen, Yunjia ; Lertwilaiwittaya, Pongtawat...
Genetics in Medicine Open.  2 (2024)  - p. 101640 , 2024
Link: https://doi.org/10.1016/..
 
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P582: CSMD1 intragenic exonic deletions strengthen the asso..:

Chen, Yunjia ; Hurst, Anna ; Seasely, Angela..
Genetics in Medicine Open.  2 (2024)  - p. 101488 , 2024
Link: https://doi.org/10.1016/..
 
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Antenatal testing surveillance and perinatal outcomes in pr..:

Page, Margaret ; Blanchard, Christina T. ; Seasely, Angela R....
American Journal of Obstetrics and Gynecology.  228 (2023)  1 - p. S184 , 2023
Link: https://doi.org/10.1016/..
 
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P440: DLG2 intragenic exonic deletions reinforce the link t..:

Chen, Yunjia ; Karaca, Ender ; Robin, Nathaniel...
Genetics in Medicine Open.  1 (2023)  1 - p. 100487 , 2023
Link: https://doi.org/10.1016/..
 
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9. Implementation survey of the ACMG/CGC standards for inte..:

Mikhail, Fady ; Biegel, Jaclyn A. ; Dubuc, Adrian M....
Cancer Genetics.  278-279 (2023)  - p. 3 , 2023
Link: https://doi.org/10.1016/..
 
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AML-430: Utility of End-of-Induction Bone Marrow Biopsy in ..:

Dunn-Valadez, Sydney ; Bathini, Srilakshmi ; Purdy, Kathleen...
Clinical Lymphoma Myeloma and Leukemia.  21 (2021)  - p. S311 , 2021
Link: https://doi.org/10.1016/..
 
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Poster: AML-430: Utility of End-of-Induction Bone Marrow Bi..:

Dunn-Valadez, Sydney ; Bathini, Srilakshmi ; Purdy, Kathleen...
Clinical Lymphoma Myeloma and Leukemia.  21 (2021)  - p. S218 , 2021
Link: https://doi.org/10.1016/..
 
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27. ACMG/CGC technical laboratory standards for interpretat..:

Raca, Gordana ; Biegel, Jaclyn ; Cooley, Linda...
Cancer Genetics.  233-234 (2019)  - p. S11 , 2019
Link: https://doi.org/10.1016/..
 
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9

Classifying and Reporting Acquired Copy Number Variants (CN..:

Raca, Gordana ; Biegel, Jaclyn ; Cooley, Linda...
Cancer Genetics.  214-215 (2017)  - p. 36-37 , 2017
Link: https://doi.org/10.1016/..
 
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10

Identification of LargeNF1Duplications Reciprocal to NAHR-M..:

Kehrer-Sawatzki, Hildegard ; Bengesser, Kathrin ; Callens, Tom...
Human Mutation.  35 (2014)  12 - p. 1469-1475 , 2014
Link: https://doi.org/10.1002/..
 
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Mosaic type-1 NF1 microdeletions as a cause of both general..:

Messiaen, Ludwine ; Vogt, Julia ; Bengesser, Kathrin...
Human Mutation.  32 (2011)  2 - p. 213-219 , 2011
Link: https://doi.org/10.1002/..
 
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Identification of SPRED1 deletions using RT‐PCR, multiplex ..:

Spencer, Emily ; Davis, Julia ; Mikhail, Fady...
American Journal of Medical Genetics Part A.  155 (2011)  6 - p. 1352-1359 , 2011
Link: https://doi.org/10.1002/..
 
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13

Section E6.1–6.6 of the American College of Medical Genetic..:

Akkari, Yassmine ; Baughn, Linda B. ; Kim, Annette...
Genetics in Medicine.  26 (2024)  4 - p. 101054 , 2024
Link: https://doi.org/10.1016/..
 
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DLG2 intragenic exonic deletions reinforce the link to neur..:

Chen, Yunjia ; Karaca, Ender ; Robin, Nathaniel H....
Genetics in Medicine.  26 (2024)  1 - p. 101010 , 2024
Link: https://doi.org/10.1016/..
 
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15

The challenges and opportunities of offering and integratin..:

Deignan, Joshua L. ; Aggarwal, Vimla ; Bale, Allen E....
Genetics in Medicine Open.  , 2024
Link: https://doi.org/10.1016/..
 
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