Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts

Yazar: Oseni, Ganiyu O., Jain, Deepti, Mossey, Peter A., Busch, Tamara D., Gowans, Lord J.J., Eshete, Mekonen A., Adeyemo, Wasiu L., Laurie, Cecelia A., Laurie, Cathy C., Owais, Arwa, Olaitan, Peter B., Aregbesola, Babatunde S., Oginni, Fadekemi O., Bello, Saidu A., Donkor, Peter, Audu, Rosemary, Onwuamah, Chika, Obiri‐Yeboah, Solomon, Plange‐Rhule, Gyikua, Ogunlewe, Olugbenga M., James, Olutayo, Halilu, Taiye, Abate, Firke, Abdur‐Rahman, Lukman O., Oladugba, Abimbola V., Marazita, Mary L., Murray, Jeffrey C., Adeyemo, Adebowale A., Butali, Azeez
Yayımlandı Mol Genet Genomic Med (2018)