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1 research outputs found
A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report
Author
AJ Carr
Aldo F. Ponce-Barahona
+36Â more
AM Elliott
Amanda G. Hernández-Padilla
Carlos A. Gámez-Fernández
Committee on Genetics
Daniel G. MartĂnez-IrĂas
Denys A. Olivera
E Haberlandt
Edwin Francisco Herrera-Paz
EN Kouwenhoven
H Lango Allen
H Saitsu
HĂ©ctor M. Ramos-ZaldĂvar
I Wieland
Isis M. Euceda
Jimena A. Montes-Gambarelli
JN Buck
JN Butcher
José S. Napky-Rajo
Julia E. Jiménez-Faraj
JW Hong
Karla G. Reyes-Perdomo
Kevin J. Robertson
KR Rosenbloom
Luis A. Leiva-Sanchez
N Tayebi
Nelson A. Espinoza-Moreno
RB Watson
RC Dale
RY Birnbaum
S Delgado
S Rattanasopha
SS Hirschfeld
SW Scherer
Tulio A. Bueso-Aguilar
Victoria A. Palomo-BermĂşdez
Wilberg A. Moncada-Arita
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
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