All individuals with variants in gene MYT1L

7 entries on 1 page. Showing entries 1 - 7.
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00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00183077 23033978-Trio92 PubMed: de Ligt 2012 - F - Netherlands - - - - - ID see paper; … 1 1 Johan den Dunnen
00308029 Pat8 PubMed: Mahler 2019 2-generation family, 1 affected, unaffected non-carrier parents - no Germany - - - - - ? moderate global developmental delay, ataxia, stereotypes 1 1 Johan den Dunnen
00402925 192392 - - F no Germany - - - - - MRD39 Generalized-onset seizure, Seizure, Obesity, Intellectual disability, severe, Intellectual disability 1 1 Andreas Laner
00407970 194348 - - F no Germany - - - - - MRD39 Delayed speech and language development, Behavioral abnormality, Global developmental delay, Neurodevelopmental delay, Urinary incontinence, Low frustration tolerance, Short attention span, Tip-toe gait 1 1 Andreas Laner
00458104 - - - M - - (not applicable) white - - - - DD HP:0001270, HP:0001252, HP:0010490 1 1 Marketa Wayhelova
00465255 326284 - - M no Germany - - - - - MRD39 Hypotonia, Delayed speech and language development, Microcephaly 1 1 Andreas Laner
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