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Willy Chertman
Willy Chertman
University of Miami
Medicine
Genetics
Exome sequencing
Nonsense mutation
Orchitis
6
Papers
5
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0
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REPRODUCTIVE ENDOCRINOLOGY AND INFERTILITY (REI) FELLOWS ARE LIKELY TO GRADUATE FROM OBGYN RESIDENCY PROGRAMS WITH REI FELLOWSHIPS
2021
Fertility and Sterility
Willy Chertman
Ranjith Ramasamy
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MP35-17 NOVEL PATHOGENIC VARIANRTS IN ALMS1 GENE IS ASSICIATED WITH PEYRONIE’S DISEASE AND DEPUYTREN’S DISEASE
2021
The Journal of Urology
Iakov V. Efimenko
Willy Chertman
Thomas A. Masterson
Anthony J. Griswold
Ranjith Ramasamy
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Whole Exome Sequencing Identifies a Rare Mutation in NACAD as a Possible Cause of COVID Orchitis in Brothers.
2021
Urology
Rohit Reddy
Iakov V. Efimenko
Willy Chertman
Taylor P. Kohn
Parris Diaz
Deepa Seetharam
Kajal Khodamoradi
Eliyahu Kresch
Ranjith Ramasamy
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Whole Exome Sequencing Identifies a Rare Nonsense Mutation in FAM47C as a Possible Cause of Severe Oligospermia in Brothers with Varicocele
2019
Urology
Willy Chertman
Himanshu Arora
Anthony Griswold
Diana M. Lopategui
Ranjith Ramasamy
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Citations (4)
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