Zobrazeno 1 - 2
of 2
pro vyhledávání: '"L A, Hosny"'
Autor:
S A, Temtamy, S, Ismail, M S, Aglan, A M, Ashour, L A, Hosny, T H, El-Badry, E H A, Aboul-Ezz, K, Amr, E, Fateen, T, Maguire, K, Ungerer, A, Zankl
Publikováno v:
Genetic counseling (Geneva, Switzerland). 23(2)
Osteolysis syndromes are rare hereditary disorders characterized by destruction and resorption of affected bones. The current study adds three new patients from two unrelated consanguineous families with a severe form of inherited osteolysis. Clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e6963cad11948541077304619e46f5d
https://pubmed.ncbi.nlm.nih.gov/22876575
https://pubmed.ncbi.nlm.nih.gov/22876575
Autor:
H H, Afifi, M O, El-Ruby, H T, El-Bassyouni, S I, Ismail, M S, Aglan, A A, El-Harouni, I M, Mazen, M S, Zaki, R I, Bassiouni, L A, Hosny, G Y, El-Kamah, A I, El-Kotoury, A M, Ashour, G M, Abdel-Salam, M A, El-Gammal, K, Hamed, R M, Kamal, I, El-Nekhely, S A, Temtamy
Publikováno v:
Bratislavske lekarske listy. 111(2)
This study presents the prevalence, relative frequency, and analysis of genetic diseases/malformations in 73260 individuals. Cases included were ascertained from: Pediatric outpatient clinics of two governmental hospitals and two primary health care
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc6d19cbb0c73131ae8cd4f7fd136b7e
https://pubmed.ncbi.nlm.nih.gov/20429316
https://pubmed.ncbi.nlm.nih.gov/20429316