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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Syndrome and CCDC28B[original query]
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly.
Journal of medical genetics 2017 11 55 (3): 189-197.
Y?ld?z Bölükba?? Esra, Mumtaz Sara, Afzal Muhammad, Woehlbier Ute, Malik Sajid, Tolun Asl?h
Clinical and Molecular Diagnosis of Joubert Syndrome and Related Disorders.
Pediatric neurology 2020 3 106 43-49.
Radha Rama Devi Akella, Naushad Shaik Mohammad, Lingappa Loke
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