APA

Faiyaz-Ul-Haque M., Zaidi S. H. E., Al-Ali M., Al-Mureikhi M. S., Kennedy S., Al-Thani G., Tsui L. & Teebi A. S. (20041222). A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type. : American journal of medical genetics. Part A.

Chicago

Faiyaz-Ul-Haque Muhammad, Zaidi Syed Hassan Ejaz, Al-Ali Mariam, Al-Mureikhi Mariam S, Kennedy Shelley, Al-Thani Ghalia, Tsui Lap-Chee and Teebi Ahmad Said. 20041222. A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type. : American journal of medical genetics. Part A.

Harvard

Faiyaz-Ul-Haque M., Zaidi S. H. E., Al-Ali M., Al-Mureikhi M. S., Kennedy S., Al-Thani G., Tsui L. and Teebi A. S. (20041222). A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type. : American journal of medical genetics. Part A.

MLA

Faiyaz-Ul-Haque Muhammad, Zaidi Syed Hassan Ejaz, Al-Ali Mariam, Al-Mureikhi Mariam S, Kennedy Shelley, Al-Thani Ghalia, Tsui Lap-Chee and Teebi Ahmad Said. A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type. : American journal of medical genetics. Part A. 20041222.