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Rare Association between Two Genetic Conditions: Turner Syndrome and Neurofibromatosis Type 1.
El Qadiry, R; Danaoui, K; Nassih, H; Bourrahouat, A; Ait Sab, I.
Affiliation
  • El Qadiry R; Pediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.
  • Danaoui K; Pediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.
  • Nassih H; Pediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.
  • Bourrahouat A; Pediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.
  • Ait Sab I; Pediatric B Department, Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco.
Case Rep Endocrinol ; 2022: 6116603, 2022.
Article in En | MEDLINE | ID: mdl-35463623
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Case Rep Endocrinol Year: 2022 Document type: Article Affiliation country: Morocco Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Case Rep Endocrinol Year: 2022 Document type: Article Affiliation country: Morocco Country of publication: United States