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Firooze Ronasian
Firooze Ronasian
Genetics
Exome sequencing
Biology
Mutation
Early Pregnancy Loss
2
Papers
26
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A homozygous NOP14 variant is likely to cause recurrent pregnancy loss
2018
Journal of Human Genetics
Toshifumi Suzuki
Mahdiyeh Behnam
Firooze Ronasian
Mansoor Salehi
Masaaki Shiina
Eriko Koshimizu
Atsushi Fujita
Futoshi Sekiguchi
Satoko Miyatake
Takeshi Mizuguchi
Mitsuko Nakashima
Kazuhiro Ogata
Satoru Takeda
Naomichi Matsumoto
Noriko Miyake
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Citations (11)
A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract.
2016
Journal of Human Genetics
Mahdiyeh Behnam
Eri Imagawa
Ahmad Reza Salehi Chaleshtori
Firooze Ronasian
Mansoor Salehi
Noriko Miyake
Naomichi Matsumoto
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Citations (15)
1