Results
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8901.
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8902.
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8903.
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8904.
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8905.
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8906.
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8907.
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8908.
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8909.
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8910.
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Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome. [electronic resource] by
- Cecchi, Alana
- Ogawa, Naomi
- Martinez, Hugo R
- Carlson, Alicia
- Fan, Yuxin
- Penny, Daniel J
- Guo, Dong-chuan
- Eisenberg, Steven
- Safi, Hazim
- Estrera, Anthony
- Lewis, Richard A
- Meyers, Deborah
- Milewicz, Dianna M
Producer: 20140326
In:
American journal of medical genetics. Part A vol. 161A
Availability: No items available.
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8911.
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8912.
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Testosterone replacement therapy to improve secondary sexual characteristics and body composition without adverse behavioral problems in adult male patients with Prader-Willi syndrome: an observational study. [electronic resource] by
- Kido, Yasuhiro
- Sakazume, Satoru
- Abe, Yoshiko
- Oto, Yuji
- Itabashi, Hisashi
- Shiraishi, Masahisa
- Yoshino, Atsunori
- Tanaka, Yuriko
- Obata, Kazuo
- Murakami, Nobuyuki
- Nagai, Toshiro
Producer: 20140326
In:
American journal of medical genetics. Part A vol. 161A
Availability: No items available.
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8913.
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8914.
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8915.
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8916.
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8917.
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8918.
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8919.
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8920.
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