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Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.
Kaya, Murat; Suer, Ilknur; Öztürk, Sükrü; Çefle, Kivanç; Karaman, Birsen; Palanduz, Sükrü.
Affiliation
  • Kaya M; Department of Medical Genetics of Internal Diseases, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
  • Suer I; Department of Medical Genetics of Internal Diseases, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
  • Öztürk S; Department of Medical Genetics of Internal Diseases, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
  • Çefle K; Department of Medical Genetics of Internal Diseases, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
  • Karaman B; Department of Medical Genetics, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
  • Palanduz S; Department of Medical Genetics of Internal Diseases, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
F1000Res ; 8: 281, 2019.
Article in En | MEDLINE | ID: mdl-31231514
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutagenesis, Insertional / Infertility, Male / Chromosome Inversion / Intellectual Disability Limits: Adult / Humans / Male Language: En Journal: F1000Res Year: 2019 Document type: Article Affiliation country: Turquía Country of publication: Reino Unido
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutagenesis, Insertional / Infertility, Male / Chromosome Inversion / Intellectual Disability Limits: Adult / Humans / Male Language: En Journal: F1000Res Year: 2019 Document type: Article Affiliation country: Turquía Country of publication: Reino Unido