All papers authored by Mira Kharbanda
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2022
Sayaka Kayumi 
,
Luis A. Pérez-Jurado,
María Palomares,
Sneha Rangu ,
Sarah E. Sheppard ,
Wendy K. Chung ,
Michael C. Kruer ,
Mira Kharbanda ,
David J. Amor ,
George McGillivray ,
Julie S. Cohen ,
Sixto García-Miñaúr,
Clare L. van Eyk ,
Kelly Harper,
Lachlan A. Jolly
and 60 other authors
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,
Luis A. Pérez-Jurado,
María Palomares,
Sneha Rangu ,
Sarah E. Sheppard ,
Wendy K. Chung ,
Michael C. Kruer ,
Mira Kharbanda ,
David J. Amor ,
George McGillivray ,
Julie S. Cohen ,
Sixto García-Miñaúr,
Clare L. van Eyk ,
Kelly Harper,
Lachlan A. Jolly
and 60 other authors
Upload
2019
Deciphering Developmental Disorders Study,
Ekaterina L. Ivanova,
Aurore Morlon,
Linyan Meng,
Anne Molitor,
Bruno Kieffer,
Nicodème Paul,
Angélique Pichot,
Frédéric Tran Mau-Them ,
Antoine Hanauer,
Lydie Naegely,
Nolwenn Jean-Marçais,
Tatiana Tvrdik,
Susan M. Hiatt,
Aline Kolmer
and 46 other authors
,
Antoine Hanauer,
Lydie Naegely,
Nolwenn Jean-Marçais,
Tatiana Tvrdik,
Susan M. Hiatt,
Aline Kolmer
and 46 other authors
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
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Mira Kharbanda ,
Daniela T. Pilz,
Susan Tomkins,
Kate Chandler,
Anand Saggar,
Alan Fryer,
Victoria McKay,
Pedro Louro,
Jill Clayton Smith,
John Burn ,
Usha Kini,
Anna De Burca,
David R. FitzPatrick,
Esther Kinning
,
Daniela T. Pilz,
Susan Tomkins,
Kate Chandler,
Anand Saggar,
Alan Fryer,
Victoria McKay,
Pedro Louro,
Jill Clayton Smith,
John Burn ,
Usha Kini,
Anna De Burca,
David R. FitzPatrick,
Esther Kinning
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals
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Davut Pehlivan,
Ka Williamson,
Stefan Johansson,
Hemant Bengani,
Luis Sanchez-Pulido,
Ja Floyd,
Mehmet Ture,
Heather Barker,
Karen Rosendahl,
Jürgen Spranger,
Ca Anderson,
Denise Horn,
Alison Meynert,
Carl A. Anderson,
Jk Rainger
and 58 other authors
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.
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