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European Journal of Medical Genetics|December 29, 2010
Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumourR A Beddow, M Smith, A Kidd, et al.
Clinical Genetics|December 1, 1982
Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33D J Tomkins, A G Hunter, I A Uchida, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 1987
Gene mapping of X-linked choroideremia with restriction fragment-length polymorphismsI M MacDonald, R M Sandre, A G Hunter, et al.
Journal of Dairy Science|December 1, 1985
Immunosuppressive activity of bovine follicular fluid on bovine T lymphocytes in vitroH A Fahmi, A G Hunter, R J Markham, et al.
Human Genetics|February 16, 1978
Geroderma osteodysplastica. A report of two affected familiesA G Hunter, J T Martsolf, C G Baker, et al.
Journal of Dairy Science|September 1, 1985
Immunosuppressive activity of bovine seminal plasma on bovine lymphocytes in vitroH A Fahmi, A G Hunter, R J Markham, et al.
Teratology|November 1, 1996
A study of level of lesion, associated malformations and sib occurrence risks in spina bifidaA G Hunter, R H Cleveland, J G Blickman, et al.
American Journal of Medical Genetics|March 1, 1990
Apparent Smith-Lemli-Opitz syndrome in a child with a previously undescribed form of mucolipidosis not involving the neuronsS Parnes, A G Hunter, C Jimenez, et al.
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