Broadening the scope of recurrent copy number variation and other congenital anomalies associated with mullerian disorders

McGowan, R., Tydeman, G.T., Shaprio, D.S., Morrison, N.M., Logan, S.L., Balen, A.B., Ahmed, F.A., Deeny, M.D., Tolmie, J.T. and Tobias, E.S.T. (2012) Broadening the scope of recurrent copy number variation and other congenital anomalies associated with mullerian disorders. Journal of Medical Genetics, 49(S1),

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Abstract

No abstract available.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:McGowan, Ruth and Tobias, Professor Edward
Authors: McGowan, R., Tydeman, G.T., Shaprio, D.S., Morrison, N.M., Logan, S.L., Balen, A.B., Ahmed, F.A., Deeny, M.D., Tolmie, J.T., and Tobias, E.S.T.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
Journal Name:Journal of Medical Genetics
Publisher:BMJ Publishing Group
ISSN:0022-2593
ISSN (Online):1468-6244
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