Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Azza E. Abd-Elnaby"'
Autor:
Hala T. El-Bassyouni, Engy A. Ashaat, Khaled Hamed, Maha Rashed, Azza E. Abd-Elnaby, Marwa Shehab
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background The hallmarks of Emanuel syndrome are pre- and postnatal growth retardation, microcephaly, global developmental delay, ear anomalies, and in males, heart, kidney, and genital abnormalities. Results This study describes the atypica
Externí odkaz:
https://doaj.org/article/eda3043060a542e784738f1cd6a26243
Autor:
Hala T. El-Bassyouni, Engy A. Ashaat, Khaled Hamed, Maha R. Abouzaid, Azza E. Abd-Elnaby, Marwa Shehab
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/036099c8e60e4564908f740610074673
Autor:
Marwa Shehab, Hala T. El-Bassyouni, Manal Abd El-Salam, Mohammed M. Sayed-Ahmed, Azza E. Abd-Elnaby, Sanaa Kamal Mohamed
Publikováno v:
Trends in Medicine. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a76e76ea015ac9ed13f0a66cbeb0523f
https://doi.org/10.15761/tim.1000238
https://doi.org/10.15761/tim.1000238
Autor:
Inas Mahfouz, Nagwa Hassan, Azza E. Abd-Elnaby, Mostafa I. Mostafa, Angie M.S. Tosson, Hala T. El-Bassyouni
Publikováno v:
J Pediatr Genet
Prader-Willi syndrome (PWS) is a distinct neurodevelopmental disorder associated with the deletion within the chromosomal 15q11-q13 region or uniparental disomy of chromosome 15. The etiologic heterogeneity of PWS makes it very difficult to establish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3f34b17002dbd7ded1825a1d57a3bf4
https://pubmed.ncbi.nlm.nih.gov/31687254
https://pubmed.ncbi.nlm.nih.gov/31687254