All individuals with variants in gene CEP104

10 entries on 1 page. Showing entries 1 - 10.
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00050250 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00363559 Fam618Pat1763,618 PubMed: Srour 2015 - F - Canada French-Canadian - - - - JBTS see paper; ... 1 1 LOVD
00363560 FamGeneDx1PatGeneDx01 PubMed: Srour 2015 - F - Canada French-Canadian - - - - JBTS see paper; ... 2 1 LOVD
00363561 FamA_IPat842629 PubMed: Srour 2015 - M - Canada French-Canadian - - - - JBTS see paper; ... 1 1 LOVD
00387835 M8800138 PubMed: Hu 2019 family, 2 or more affected individuals, first cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, no microcephaly 1 2 Johan den Dunnen
00387902 M9100012 PubMed: Hu 2019 family, 3 affected individuals, first cousin parents - yes - Lur - - - - ID non-syndromic intellectual disability, no microcephaly 1 3 Johan den Dunnen
00418597 Fam3PatIV1 PubMed: Bertoli-Avella 2022 4-generation family, 3 affected (3M), unaffected heterozygous carrier parents/relatives M yes Iraq - - - - - CF failure to thrive, weight, height and ofc below 5th percentile; no dysmorphism; mild motor delay; normal mental development; no neurological abnormalities; recurrent lower respiratory tract infections; mild respiratory tract infections; no immunological abnormalities; chronic diarrhea, episodic vomiting, lethargy; no cardiovascular abnormalities 1 3 Johan den Dunnen
00441570 B00APG4 PubMed: Boucher 2020 - - - France - - - - - HL - 1 1 Johan den Dunnen
00462324 Pat9 PubMed: Alsamri 2021 analysis 66 patients with significant clinical respiratory problems; 2-generation family, 1 affected, unaffected heterozygous carrier parents - - United Arab Emirates - - - - - CILD Joubert syndrome 1 1 Johan den Dunnen
00466456 Pat1 PubMed: Takata 2014, Journal: Takata 2014 2-generation family, 1 affected, unaffected non-carrier paren - - United States white - - - - SCZD - 1 1 Johan den Dunnen
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