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AJA.AJA_32_17
AJA.AJA_32_17
http://dx.doi.org/10.4103/AJA.AJA_32_17
A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome.
P356
Q47735813-0453515B-8549-423B-B80F-05E5B9DA9920
P356
AJA.AJA_32_17
http://dx.doi.org/10.4103/AJA.AJA_32_17