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A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.
Elhossini, Rasha M; Sayed, Inas M; Hellal, Usama Saad; Mahmoud, Sarah A M; Aglan, Mona S; Hassib, Nehal F; Abdel-Hamid, Mohamed S.
Affiliation
  • Elhossini RM; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
  • Sayed IM; Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
  • Hellal US; Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
  • Mahmoud SAM; Oral & Maxillofacial Pathology Department, Faculty of Dentistry, Cairo University, Cairo, Egypt.
  • Aglan MS; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
  • Hassib NF; Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
  • Abdel-Hamid MS; School of Dentistry, New Giza University, Giza, Egypt.
Am J Med Genet A ; 194(1): 39-45, 2024 Jan.
Article in En | MEDLINE | ID: mdl-37750049
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gingival Overgrowth / Fibromatosis, Gingival / Hypertrichosis / Intellectual Disability Limits: Humans / Male Language: En Journal: Am J Med Genet A Year: 2024 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gingival Overgrowth / Fibromatosis, Gingival / Hypertrichosis / Intellectual Disability Limits: Humans / Male Language: En Journal: Am J Med Genet A Year: 2024 Document type: Article