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An Lu(a-b-) Phenotype Caused by an X-Linked Recessive Gene

✍ Scribed by P.C. Norman; P. Tippett; R. W. Beal


Book ID
115108999
Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
296 KB
Volume
51
Category
Article
ISSN
0042-9007

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A patient with an interstitial deletion
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A male patient carrying an interstitial deletion in Xp22.3 and affected by Kallmann syndrome, X-linked ichthyosis and mental retardation, but without chondrodysplasia punctata or short stature, was investigated with molecular probes from the distal Xp22.3 region. By means of a novel probe, M115, fro