Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Anisa Saad"'
Autor:
C. Bensignor, Yosra Halleb, A. Tej, A. Touati, A. Ben Ahmed, S. Kmiha, D. H’mida Ben Brahim, N. Mahdhaoui, Anisa Saad, Sonia Nouri, J. Mathlouthi
Publikováno v:
Archives de Pédiatrie. 26:102-107
Background and objectives Sanjad–Sakati syndrome (SSS; OMIM 241410) is a rare autosomal recessive disorder found almost exclusively in people of Arab origin. It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d44ff8d7d0c12b176780f88632f2654f
https://doi.org/10.1016/j.arcped.2018.11.012
https://doi.org/10.1016/j.arcped.2018.11.012
Autor:
Robert Oseasohn, Saiyid Rizvi, Anisa Saad, William B. Greenough, Abram S. Benenson, John Lindenbaum
Publikováno v:
The Lancet. 285:1081-1083
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42917a8cdbf3d5795401711031345955
https://doi.org/10.1016/s0140-6736(65)92671-1
https://doi.org/10.1016/s0140-6736(65)92671-1