All individuals with variants in gene FRMD4A

2 entries on 1 page. Showing entries 1 - 2.
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00017840 - PubMed: Fine 2015, Journal: Fine 2015 5-generation family, 6 affected (2F, 3M, 1 fetus), unaffected heterozygous carrier parents/relatives F;M yes Israel Bedouin - - - - ? intellectual disability syndrome of congenital microcephaly, low anterior hairline, bitemporal narrowing, low-set protruding ears, strabismus and tented thick eyebrows with sparse hair in their medial segment. 1 3 Ohad S Birk
00426124 10BS10100 PubMed: Al-Kasbi 2022 patient, no other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
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