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Two new families with enamel renal syndrome: A novel FAM20A gene mutation and review of literature.
Hassib, Nehal F; Shoeib, Mona A; ElSadek, Hoda A; Wali, Mona E; Mostafa, Mostafa I; Abdel-Hamid, Mohamed S.
Affiliation
  • Hassib NF; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Shoeib MA; Oral Medicine & Periodontology Department, Faculty of Oral & Dental Medicine, Cairo University, Egypt.
  • ElSadek HA; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Wali ME; Oral Pathology Department, Faculty of Dentistry, Cairo University, Egypt.
  • Mostafa MI; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Abdel-Hamid MS; Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt. Electronic address: mohamadnrc@hotmail.com.
Eur J Med Genet ; 63(11): 104045, 2020 Nov.
Article in En | MEDLINE | ID: mdl-32835847
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dental Enamel Proteins / Amelogenesis Imperfecta / Nephrocalcinosis Type of study: Prognostic_studies Limits: Adolescent / Female / Humans / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Egypt Country of publication: Netherlands
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dental Enamel Proteins / Amelogenesis Imperfecta / Nephrocalcinosis Type of study: Prognostic_studies Limits: Adolescent / Female / Humans / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Egypt Country of publication: Netherlands