All individuals with variants in gene SYT1

6 entries on 1 page. Showing entries 1 - 6.
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Owner     
00019920 - PubMed: Cafiero 2015, Journal: Cafiero 2015 - F no Italy white >04y - - - ID Developmental delay, absent speech, EEG anomalies, hypotonia, esotropia, hypertrichosis 1 1 Giuseppe Marangi
00132291 FamPatIV2 PubMed: Eisenberger 2018 4-generation family, 8 affected (4F, 4M) M no Germany white - - - - DFNA see paper; ... 1 8 Hanno Bolz
00392042 216P - - M no Spain - - - - - ID - 1 1 Alejandro Brea-Fernández
00409219 196814 - - M no Germany - - - - - BAGOS Neurodevelopmental delay, Autistic behavior, Absent speech, Developmental regression, Enuresis, Encopresis, Hypermetropia, Short stature, Hypotonia, neonatal 1 1 Andreas Laner
00446556 - - - F no Spain white - - - - BAGOS - 1 1 Francisco Martínez-Azorín
00464287 Pat2 PubMed: Izumi 2016, Journal: Izumi 2016 2-generation family, 1 affected, unaffected non carrier parents M - Singapore - - - - - ? see paper; ..., intrauterine growth retardation; micrognathia; no cleft palate; tracheostomy; no congenital heart disease; cryptorchidism; short stature; no rhizomelic shortening; joint laxity; developmental delay; autism; seizure; no microcephaly 1 1 Johan den Dunnen
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