Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances. [electronic resource]

By:

Doornbos, Marianne

Contributor(s):

Sikkema-Raddatz, Birgit
Ruijvenkamp, Claudia A L
Dijkhuizen, Trijnie
Bijlsma, Emilia K
Gijsbers, Antoinet C J
Hilhorst-Hofstee, Yvonne
Hordijk, Roel
Verbruggen, Krijn T
Kerstjens-Frederikse, W S Mieke
van Essen, Ton
Kok, Klaas
van Silfhout, Anneke T
Breuning, Martijn
van Ravenswaaij-Arts, Conny M A

Producer: 20090901Description: 108-15 p. digitalISSN:

1878-0849

Subject(s):

Angelman Syndrome -- genetics
Child
Child, Preschool
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders -- genetics
Chromosomes, Human, Pair 15
Family Health
Humans
Male
Mental Disorders -- genetics
Prader-Willi Syndrome -- genetics
Speech Disorders
Syndrome

Online resources:

Available from publisher's website

In: European journal of medical genetics vol. 52

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Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances.

APA

Doornbos M., Sikkema-Raddatz B., Ruijvenkamp C. A. L., Dijkhuizen T., Bijlsma E. K., Gijsbers A. C. J., Hilhorst-Hofstee Y., Hordijk R., Verbruggen K. T., Kerstjens-Frederikse W. S. M., van Essen T., Kok K., van Silfhout A. T., Breuning M. & van Ravenswaaij-Arts C. M. A. (20090901). Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances. : European journal of medical genetics.

Chicago

Doornbos Marianne, Sikkema-Raddatz Birgit, Ruijvenkamp Claudia A L, Dijkhuizen Trijnie, Bijlsma Emilia K, Gijsbers Antoinet C J, Hilhorst-Hofstee Yvonne, Hordijk Roel, Verbruggen Krijn T, Kerstjens-Frederikse W S Mieke, van Essen Ton, Kok Klaas, van Silfhout Anneke T, Breuning Martijn and van Ravenswaaij-Arts Conny M A. 20090901. Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances. : European journal of medical genetics.

Harvard

Doornbos M., Sikkema-Raddatz B., Ruijvenkamp C. A. L., Dijkhuizen T., Bijlsma E. K., Gijsbers A. C. J., Hilhorst-Hofstee Y., Hordijk R., Verbruggen K. T., Kerstjens-Frederikse W. S. M., van Essen T., Kok K., van Silfhout A. T., Breuning M. and van Ravenswaaij-Arts C. M. A. (20090901). Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances. : European journal of medical genetics.

MLA

Doornbos Marianne, Sikkema-Raddatz Birgit, Ruijvenkamp Claudia A L, Dijkhuizen Trijnie, Bijlsma Emilia K, Gijsbers Antoinet C J, Hilhorst-Hofstee Yvonne, Hordijk Roel, Verbruggen Krijn T, Kerstjens-Frederikse W S Mieke, van Essen Ton, Kok Klaas, van Silfhout Anneke T, Breuning Martijn and van Ravenswaaij-Arts Conny M A. Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances. : European journal of medical genetics. 20090901.

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