All individuals with variants in gene PCDHB4

4 entries on 1 page. Showing entries 1 - 4.
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AscendingIndividual ID     

ID_report     

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Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

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Disease     

Phenotype details     

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Panel size     

Owner     
00050575 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, seizures 1 1 Johan den Dunnen
00225691 25558065-Fam10DG1069 PubMed: Alazami 2015, Journal: Alazami 2015 4-generation family, 2 affected (F, M), unaffected heterozygous carrier parents/relatives F;M yes Saudi Arabia - - - - - ? see paper; …, primary microcephaly and global developmental delay 1 2 Johan den Dunnen
00361555 10DG1069 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; global developmental delay, primary microcephaly 1 1 Johan den Dunnen
00361571 12DG1068 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; intellectual disability, microcephaly 1 1 Johan den Dunnen
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