Title : Autozygome and high throughput confirmation of disease genes candidacy - Maddirevula_2019_Genet.Med_21_736 |
Author(s) : Maddirevula S , Alzahrani F , Al-Owain M , Al Muhaizea MA , Kayyali HR , AlHashem A , Rahbeeni Z , Al-Otaibi M , Alzaidan HI , Balobaid A , El Khashab HY , Bubshait DK , Faden M , Yamani SA , Dabbagh O , Al-Mureikhi M , Jasser AA , Alsaif HS , Alluhaydan I , Seidahmed MZ , Alabbasi BH , Almogarri I , Kurdi W , Akleh H , Qari A , Al Tala SM , Alhomaidi S , Kentab AY , Salih MA , Chedrawi A , Alameer S , Tabarki B , Shamseldin HE , Patel N , Ibrahim N , Abdulwahab F , Samira M , Goljan E , Abouelhoda M , Meyer BF , Hashem M , Shaheen R , AlShahwan S , Alfadhel M , Ben-Omran T , Al-Qattan MM , Monies D , Alkuraya FS |
Ref : Genet Med , 21 :736 , 2019 |
Abstract : Maddirevula_2019_Genet.Med_21_736 |
ESTHER : Maddirevula_2019_Genet.Med_21_736 |
PubMedSearch : Maddirevula_2019_Genet.Med_21_736 |
PubMedID: 30237576 |
Maddirevula S, Alzahrani F, Al-Owain M, Al Muhaizea MA, Kayyali HR, AlHashem A, Rahbeeni Z, Al-Otaibi M, Alzaidan HI, Balobaid A, El Khashab HY, Bubshait DK, Faden M, Yamani SA, Dabbagh O, Al-Mureikhi M, Jasser AA, Alsaif HS, Alluhaydan I, Seidahmed MZ, Alabbasi BH, Almogarri I, Kurdi W, Akleh H, Qari A, Al Tala SM, Alhomaidi S, Kentab AY, Salih MA, Chedrawi A, Alameer S, Tabarki B, Shamseldin HE, Patel N, Ibrahim N, Abdulwahab F, Samira M, Goljan E, Abouelhoda M, Meyer BF, Hashem M, Shaheen R, AlShahwan S, Alfadhel M, Ben-Omran T, Al-Qattan MM, Monies D, Alkuraya FS (2019)
Autozygome and high throughput confirmation of disease genes candidacy
Genet Med
21 :736
Maddirevula S, Alzahrani F, Al-Owain M, Al Muhaizea MA, Kayyali HR, AlHashem A, Rahbeeni Z, Al-Otaibi M, Alzaidan HI, Balobaid A, El Khashab HY, Bubshait DK, Faden M, Yamani SA, Dabbagh O, Al-Mureikhi M, Jasser AA, Alsaif HS, Alluhaydan I, Seidahmed MZ, Alabbasi BH, Almogarri I, Kurdi W, Akleh H, Qari A, Al Tala SM, Alhomaidi S, Kentab AY, Salih MA, Chedrawi A, Alameer S, Tabarki B, Shamseldin HE, Patel N, Ibrahim N, Abdulwahab F, Samira M, Goljan E, Abouelhoda M, Meyer BF, Hashem M, Shaheen R, AlShahwan S, Alfadhel M, Ben-Omran T, Al-Qattan MM, Monies D, Alkuraya FS (2019)
Genet Med
21 :736