Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.
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Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.
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(P356) |
10.1056/NEJM197405162902001
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(P698) |
4821173
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(P8608) |
release_fqw2uvepifgkxk3pgpeh7u5oaa
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