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Rebecca Miller

RM

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Publications

1

Citations

38

H-Index

1

Active since

2018

Affiliations

Istanbul Bilim University(Current)

Rebecca Miller is an author at Istanbul Bilim University specializing in intellectual disability genetics, missense mutations, and genetic neurodevelopmental syndromes.

Publications per year

2018–2018

1

Publications

1

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive <i>c</i>erebellar, <i>o</i>cular, cranio<i>f</i>acial and <i>g</i>enital features (COFG syndrome)

Abolfazl Rad, Umut Altunoğlu, Rebecca Miller et al. · Journal of Medical Genetics · 2018 · 38 citations · Full text

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