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Publications by S J Davies

Marfan Syndrome: Fibrillin Expression and Microfibrillar Abnormalities in a Family With Predominant Ocular Defects.

Journal of Medical Genetics
Genetics
1995English

Bilateral Split Hand and Split Foot Malformation in a Boy With a De Novo Interstitial Deletion of 7q21.3

Journal of Medical Genetics
Genetics
1991English

Cutis Laxa: A Feature of Costello Syndrome.

Journal of Medical Genetics
Genetics
1994English

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