All individuals with variants in gene HOXD13

6 entries on 1 page. Showing entries 1 - 6.
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00079981 - PubMed: Jamsheer 2012 2-generation family, 2 affected (proband: daughter; father) F;M - Poland European - - - - BDE2 - 1 2 Arrate Pereda
00079982 - PubMed: Johnson 2003 4-generation family, 12 affecteds (only 9 individuals examined: 6F, 3M) F;M - (United Kingdom (Great Britain)) - - - - - BDD, BDE2 - 1 12 Arrate Pereda
00079983 - PubMed: Johnson 2003 4-generation family, 8 affecteds (6F, 2M) F;M - (United Kingdom (Great Britain)) - - - - - BDD, BDE2 - 1 8 Arrate Pereda
00079984 - PubMed: Johnson 2003 3-generation family, 8 affecteds (only 7 individuals examined 4F, 3M) F;M - (United Kingdom (Great Britain)) - - - - - BDD, BDE2 - 1 8 Arrate Pereda
00316093 K126 PubMed: Heidet 2017 fetus - - France - - - - - CAKUT bilateral kidney agenesis 1 1 Johan den Dunnen
00443881 FamFPatIV1 PubMed: Chatron 2020 3-generation family, 1 affected brother, unaffected heterozygous parents/relatives F yes Brazil - - - - - DEE see paper; ..., 7d-myoclonic seizure; tonic seizures, epileptic spasms, focal seizures; EEG at onset suppression-burst pattern; occasional seizure; dystonia and hyperkinetic movements; profound intellectual disability; no pes equinovarus; no omphalocele; no cleft palate; joint contractures; no dysmorphic facial features; MRI brain 4m-normal, 13m-mild cerebral atrophy, 6y-mild cerebral atrophy with ventricular dilation 1 1 Johan den Dunnen
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