Search

Author/Creator Meyer, Brian

2. A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies. Issue 1 (December 2016)

Authors:
Monies, Dorota; Alhindi, Hindi; Almuhaizea, Mohamed; Abouelhoda, Mohamed; Alazami, Anas; Goljan, Ewa; Alyounes, Banan; Jaroudi, Dyala; AlIssa, Abdulelah; Alabdulrahman, Khalid; Subhani, Shazia; El-Kalioby, Mohamed; Faquih, Tariq; Wakil, Salma; Altassan, Nada; Meyer, Brian; Bohlega, Saeed
Journal:
Human genomics
Issue:
Volume 10:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Developing a Computer Touch-Screen Interactive Colorectal Screening Decision Aid for a Low-Literacy African American Population: Lessons Learned. Issue 4 (July 2013)

Authors:
Bass, Sarah Bauerle; Gordon, Thomas F.; Ruzek, Sheryl Burt; Wolak, Caitlin; Ruggieri, Dominique; Mora, Gabriella; Rovito, Michael J.; Britto, Johnson; Parameswaran, Lalitha; Abedin, Zainab; Ward, Stephanie; Paranjape, Anuradha; Lin, Karen; Meyer, Brian; Pitts, Khaliah
Journal:
Health promotion practice
Issue:
Volume 14:Issue 4(2013)
Page Start:
589
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype. Issue 4 (22nd March 2017)

Authors:
Altassan, Ruqaiah; Saud, Haya Al; Masoodi, Tariq Ahmad; Dosssari, Haya Al; Khalifa, Ola; Al‐Zaidan, Hamad; Sakati, Nadia; Rhabeeni, Zuhair; Al‐Hassnan, Zuhair; Binamer, Yousef; Alhashemi, Nadia; Wade, William; Al‐Zayed, Zayed; Al‐Sayed, Moeen; Al‐Muhaizea, Mohamed A.; Meyer, Brian; Al‐Owain, Moha...
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 4(2017)
Page Start:
1009
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene. (12th December 2018)

Authors:
Wakil, Salma M.; Monies, Dorota; Hagos, Samya; Al-Ajlan, Fahad; Finsterer, Josef; Al Qahtani, Aisha; Ramzan, Khushnooda; Al Humaidy, Rawan; Al-Muhaizea, Mohamed A.; Meyer, Brian; Bohlega, Saeed A.
Other Names:
Paracchini Silvia Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2018(2018)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel. Issue 5 (9th February 2016)

Authors:
Al-Hamed, Mohamed H; Kurdi, Wesam; Alsahan, Nada; Alabdullah, Zainab; Abudraz, Rania; Tulbah, Maha; Alnemer, Maha; Khan, Rubina; Al-Jurayb, Haya; Alahmed, Ahmed; Tahir, Asma I; Khalil, Dania; Edwards, Noel; Al Abdulaziz, Basma; Binhumaid, Faisal S; Majid, Salma; Faquih, Tariq; El-Kalioby, Mohamed...
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 5(2016)
Page Start:
338
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability. Issue 11 (31st August 2016)

Authors:
Kaya, Namik; Alsagob, Maysoon; D'Adamo, Maria Cristina; Al-Bakheet, Albandary; Hasan, Sonia; Muccioli, Maria; Almutairi, Faten B; Almass, Rawan; Aldosary, Mazhor; Monies, Dorota; Mustafa, Osama M; Alyounes, Banan; Kenana, Rosan; Al-Zahrani, Jawaher; Naim, Eva; Binhumaid, Faisal S; Qari, Alya; Alm...
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 11(2016)
Page Start:
786
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗