APA
Walters R. G., Jacquemont S., Valsesia A., de Smith A. J., Martinet D., Andersson J., Falchi M., Chen F., Andrieux J., Lobbens S., Delobel B., Stutzmann F., El-Sayed Moustafa J. S., Chèvre J., Lecoeur C., Vatin V., Bouquillon S., Buxton J. L., Boute O., Holder-Espinasse M., Cuisset J., Lemaitre M., Ambresin A., Brioschi A., Gaillard M., Giusti V., Fellmann F., Ferrarini A., Hadjikhani N., Campion D., Guilmatre A., Goldenberg A., Calmels N., Mandel J., Le Caignec C., David A., Isidor B., Cordier M., Dupuis-Girod S., Labalme A., Sanlaville D., Béri-Dexheimer M., Jonveaux P., Leheup B., Ounap K., Bochukova E. G., Henning E., Keogh J., Ellis R. J., Macdermot K. D., van Haelst M. M., Vincent-Delorme C., Plessis G., Touraine R., Philippe A., Malan V., Mathieu-Dramard M., Chiesa J., Blaumeiser B., Kooy R. F., Caiazzo R., Pigeyre M., Balkau B., Sladek R., Bergmann S., Mooser V., Waterworth D., Reymond A., Vollenweider P., Waeber G., Kurg A., Palta P., Esko T., Metspalu A., Nelis M., Elliott P., Hartikainen A., McCarthy M. I., Peltonen L., Carlsson L., Jacobson P., Sjöström L., Huang N., Hurles M. E., O'Rahilly S., Farooqi I. S., Männik K., Jarvelin M., Pattou F., Meyre D., Walley A. J., Coin L. J. M., Blakemore A. I. F., Froguel P. & Beckmann J. S. (20100312). A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. : Nature.
Chicago
Walters R G, Jacquemont S, Valsesia A, de Smith A J, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa J S, Chèvre J-C, Lecoeur C, Vatin V, Bouquillon S, Buxton J L, Boute O, Holder-Espinasse M, Cuisset J-M, Lemaitre M-P, Ambresin A-E, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, Guilmatre A, Goldenberg A, Calmels N, Mandel J-L, Le Caignec C, David A, Isidor B, Cordier M-P, Dupuis-Girod S, Labalme A, Sanlaville D, Béri-Dexheimer M, Jonveaux P, Leheup B, Ounap K, Bochukova E G, Henning E, Keogh J, Ellis R J, Macdermot K D, van Haelst M M, Vincent-Delorme C, Plessis G, Touraine R, Philippe A, Malan V, Mathieu-Dramard M, Chiesa J, Blaumeiser B, Kooy R F, Caiazzo R, Pigeyre M, Balkau B, Sladek R, Bergmann S, Mooser V, Waterworth D, Reymond A, Vollenweider P, Waeber G, Kurg A, Palta P, Esko T, Metspalu A, Nelis M, Elliott P, Hartikainen A-L, McCarthy M I, Peltonen L, Carlsson L, Jacobson P, Sjöström L, Huang N, Hurles M E, O'Rahilly S, Farooqi I S, Männik K, Jarvelin M-R, Pattou F, Meyre D, Walley A J, Coin L J M, Blakemore A I F, Froguel P and Beckmann J S. 20100312. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. : Nature.
Harvard
Walters R. G., Jacquemont S., Valsesia A., de Smith A. J., Martinet D., Andersson J., Falchi M., Chen F., Andrieux J., Lobbens S., Delobel B., Stutzmann F., El-Sayed Moustafa J. S., Chèvre J., Lecoeur C., Vatin V., Bouquillon S., Buxton J. L., Boute O., Holder-Espinasse M., Cuisset J., Lemaitre M., Ambresin A., Brioschi A., Gaillard M., Giusti V., Fellmann F., Ferrarini A., Hadjikhani N., Campion D., Guilmatre A., Goldenberg A., Calmels N., Mandel J., Le Caignec C., David A., Isidor B., Cordier M., Dupuis-Girod S., Labalme A., Sanlaville D., Béri-Dexheimer M., Jonveaux P., Leheup B., Ounap K., Bochukova E. G., Henning E., Keogh J., Ellis R. J., Macdermot K. D., van Haelst M. M., Vincent-Delorme C., Plessis G., Touraine R., Philippe A., Malan V., Mathieu-Dramard M., Chiesa J., Blaumeiser B., Kooy R. F., Caiazzo R., Pigeyre M., Balkau B., Sladek R., Bergmann S., Mooser V., Waterworth D., Reymond A., Vollenweider P., Waeber G., Kurg A., Palta P., Esko T., Metspalu A., Nelis M., Elliott P., Hartikainen A., McCarthy M. I., Peltonen L., Carlsson L., Jacobson P., Sjöström L., Huang N., Hurles M. E., O'Rahilly S., Farooqi I. S., Männik K., Jarvelin M., Pattou F., Meyre D., Walley A. J., Coin L. J. M., Blakemore A. I. F., Froguel P. and Beckmann J. S. (20100312). A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. : Nature.
MLA
Walters R G, Jacquemont S, Valsesia A, de Smith A J, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa J S, Chèvre J-C, Lecoeur C, Vatin V, Bouquillon S, Buxton J L, Boute O, Holder-Espinasse M, Cuisset J-M, Lemaitre M-P, Ambresin A-E, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, Guilmatre A, Goldenberg A, Calmels N, Mandel J-L, Le Caignec C, David A, Isidor B, Cordier M-P, Dupuis-Girod S, Labalme A, Sanlaville D, Béri-Dexheimer M, Jonveaux P, Leheup B, Ounap K, Bochukova E G, Henning E, Keogh J, Ellis R J, Macdermot K D, van Haelst M M, Vincent-Delorme C, Plessis G, Touraine R, Philippe A, Malan V, Mathieu-Dramard M, Chiesa J, Blaumeiser B, Kooy R F, Caiazzo R, Pigeyre M, Balkau B, Sladek R, Bergmann S, Mooser V, Waterworth D, Reymond A, Vollenweider P, Waeber G, Kurg A, Palta P, Esko T, Metspalu A, Nelis M, Elliott P, Hartikainen A-L, McCarthy M I, Peltonen L, Carlsson L, Jacobson P, Sjöström L, Huang N, Hurles M E, O'Rahilly S, Farooqi I S, Männik K, Jarvelin M-R, Pattou F, Meyre D, Walley A J, Coin L J M, Blakemore A I F, Froguel P and Beckmann J S. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. : Nature. 20100312.