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Author/Creator Cunningham, Mitch

1. Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1. Issue 1 (26th October 2019)

Authors:
Koczkowska, Magdalena; Callens, Tom; Chen, Yunjia; Gomes, Alicia; Hicks, Alesha D.; Sharp, Angela; Johns, Eric; Uhas, Kim Armfield; Armstrong, Linlea; Bosanko, Katherine Armstrong; Babovic‐Vuksanovic, Dusica; Baker, Laura; Basel, Donald G.; Bengala, Mario; Bennett, James T.; Chambers, Chelsea; Cl...
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
299
Record Type:
Journal Article
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2. Delineating the genotypic and phenotypic spectrum of HECW2-related neurodevelopmental disorders. Issue 7 (28th July 2021)

Authors:
Acharya, Anushree; Kavus, Haluk; Dunn, Patrick; Nasir, Abdul; Folk, Leandra; Withrow, Kara; Wentzensen, Ingrid M.; Ruzhnikov, Maura R. Z.; Fallot, Camille; Smol, Thomas; Rama, Mélanie; Brown, Kathleen; Whalen, Sandra; Ziegler, Alban; Barth, Magali; Chassevent, Anna; Smith-Hicks, Constance; Afenja...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 7(2022)
Page Start:
669
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Summary report of the 2019 Diversity and Inclusion Task Force of the National Society of Genetic Counselors. Issue 2 (30th March 2020)

Authors:
Channaoui, Nadine; Khan, Ambreen; Wiesman, Chana; Bui, Kara; Cunningham, Mitch; Brown, Kaitlyn; Wolfe Schneider, Kami; Platt, Kristal; Hodges, Priscila Delgado; Thompson, Nicole; Haas, Bruce; Strang, Katie; Carey, Meghan; Ramos, Erica; Arjunan, Aishwarya; Platt, Julia
Journal:
Journal of genetic counseling
Issue:
Volume 29:Issue 2(2020)
Page Start:
192
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗