Results 141 to 146 of about 2,857 (146)

Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family. [PDF]

Mol Genet Genomic Med
Abosabie SAS, Abosabie SA, Alfaifi J, Alqahtani YA, Shati AA, Alotaibi NA, Alghamdi OA, Alotaibi GN, Baabdullah AA, Kabrah LK, Kamal NM, Oshi MAM, Abdallah EAA.   +12 more
europepmc   +1 more source

Alstrom syndrome in four sibs from northern Jordan

Annals of Saudi Medicine, 2006
Hamamy Hanan, Barham Muries, Alkhawaldeh Abd-ElKarim, Cockburn David, Snowden Helen, Ajlouni Kamel   +5 more
doaj