Zobrazeno 1 - 2
of 2
pro vyhledávání: '"O, Mouhib Lav"'
Autor:
Hanane, Latrech, Imane, Skiker, Yassamine, Bentata, Zayneb, Alami, O, Mouhib Lav, Oumnia Mouhib, Lah, Nouredine, Oulali, Nouffissa, Benajiba, S, Benmassoud, Mohammed, El Jabri, Ahmed, Gaouzi, M H, Gharbi, Mohammed El Hassan, Gharbi, Abdelmjid, Chradibi
Publikováno v:
Pediatric endocrinology reviews : PER. 11(2)
Dyggve-Melchiore-Clausen (DMC) syndrome is a are autosomal recessive spondyloepimetaphyseal dysplasia associated with mental retardation resulting from mutations in the Dymeclin (DYM) gene mapped in the 18q12-12.1 chromosomal region. We report a case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc286fd587e7132c5305100ff05e6ce7
https://pubmed.ncbi.nlm.nih.gov/24575553
https://pubmed.ncbi.nlm.nih.gov/24575553
Autor:
Latrech H; Department of Endocrinology, Medical School, University Mohamed First, Oujda, Morocco. hlatrech@hotmail.com, Skiker I; Department of Radiology, Medical School, University Mohamed First, Oujda, Morocco., Bentata Y; Department of Nephrology, Medical School, University Mohamed First, Oujda, Morocco., Alami Z; Pharmacology, Medical School, University Mohamed First, Oujda, Morocco., Mouhib Lav O, Oulali N; Department of Neurosurgery, Medical School, University Mohamed First, Oujda, Morocco., Benajiba N; Department of Pediatrics, Medical School, University Mohamed First, Oujda, Morocco., Benmassoud S; Department of Pediatrics, Medical School, University Mohamed First, Oujda, Morocco., El Jabri M; Department of Pediatrics, Medical School, University Mohamed First, Oujda, Morocco., Gaouzi A; Department of Endocrinology Pediatrics, Medical School, University Mohamed V, Rabat, Morocco., Gharbi MH, Chradibi A; Department of Endocrinology, Medical School, University Mohamed V, Ibn Sina hospital, Rabat, Morocco.
Publikováno v:
Pediatric endocrinology reviews : PER [Pediatr Endocrinol Rev] 2013 Dec; Vol. 11 (2), pp. 181-5.