Zobrazeno 1 - 2
of 2
pro vyhledávání: '"M A Abdel Rasool"'
Autor:
W. Al-Busairi, M. Hassan, M. Rudwan, A. J. Khuraibet, S. Elgamal, Talaat I. Farag, S. Khaffagi, S J Abulhassan, B. Qasrawi, N. Haseeb, S. Farah, Mohamed Sabry, M. A. Abdel-Rasool
Publikováno v:
Clinical Genetics. 51:326-330
Clinico-radiological assessment of three mentally retarded members of a large Bedouin kindred showed lissencephaly, spastic paraparesis, myoclonic epilepsy and cerebellar hypoplasia. It seems that the familial association of lissencephaly/myoclonic e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ad97f77908f32f057587b5826a5dfd
https://doi.org/10.1111/j.1399-0004.1997.tb02482.x
https://doi.org/10.1111/j.1399-0004.1997.tb02482.x
Autor:
M. Zaki, S. A. Al Awadi, M A Abdel Rasool, S J Abul Hassan, Dina Ramadan, Mohamed Sabry, Q. Al Saleh
We report four sibs with Kenny-Caffey syndrome in a consanguineous Bedouin family. The first two died in the neonatal period while the remaining affected brother and sister had all the characteristic clinical, biochemical, and radiological abnormalit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9610500351cfc7530e95a960ea0e918c
https://europepmc.org/articles/PMC1051183/
https://europepmc.org/articles/PMC1051183/
