All individuals with variants in gene DMXL2

5 entries on 1 page. Showing entries 1 - 5.
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Owner     
00301710 17-4220 PubMed: Maddirevula 2019 - M - - - - - - - ? focal seizures at age 3 months (admitted for 2 months in PICU). Since then, he was noted to have global developmental delay, no eye contact, moderate degree of cerebral atrophy, macrocephaly and dysmorphic features (long face, high forehead, short philtrum and low set ears). Brain MRI revealed moderate degree of cerebral atrophy including atrophy of the brainstem. Parents are healthy first cousins with no similarly affected children. 1 1 Johan den Dunnen
00436675 - - - rM - - - - - - - DSD - 1 1 Kenneth Mcelreavey
00441510 B00APG2 PubMed: Boucher 2020 - - - France - - - - - HL - 1 1 Johan den Dunnen
00441511 6586 PubMed: Boucher 2020 - - - France - - - - - HL - 1 1 Johan den Dunnen
00441547 33004-4 PubMed: Boucher 2020 control - - France - - - - - Healthy/Control - 1 1 Johan den Dunnen
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