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381.
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383.
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Augmentation index and the evolution of aortic disease in marfan-like syndromes. [electronic resource] by
- Mortensen, Kai
- Baulmann, Johannes
- Rybczynski, Meike
- Sheikhzadeh, Sara
- Aydin, Muhammet A
- Treede, Henrik
- Dombrowski, Ellen
- Kühne, Kristin
- Peitsmeier, Philipp
- Habermann, Christian R
- Robinson, Peter N
- Stuhrmann, Manfred
- Berger, Jürgen
- Meinertz, Thomas
- von Kodolitsch, Yskert
Producer: 20100923
In:
American journal of hypertension vol. 23
Availability: No items available.
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384.
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385.
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Latent TGF-β binding protein-2 is essential for the development of ciliary zonule microfibrils. [electronic resource] by
- Inoue, Tadashi
- Ohbayashi, Tetsuya
- Fujikawa, Yusuke
- Yoshida, Hideyuki
- Akama, Tomoya O
- Noda, Kazuo
- Horiguchi, Masahito
- Kameyama, Katsuro
- Hata, Yoshio
- Takahashi, Kanji
- Kusumoto, Kenji
- Nakamura, Tomoyuki
Producer: 20150610
In:
Human molecular genetics vol. 23
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386.
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387.
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388.
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389.
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Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [electronic resource] by
- Morales, Jose
- Al-Sharif, Latifa
- Khalil, Dania S
- Shinwari, Jameela M A
- Bavi, Prashant
- Al-Mahrouqi, Rahima A
- Al-Rajhi, Ali
- Alkuraya, Fowzan S
- Meyer, Brian F
- Al Tassan, Nada
Producer: 20091222
In:
American journal of human genetics vol. 85
Availability: No items available.
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390.
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391.
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A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome. [electronic resource] by
- Yin, Y
- Liu, X-H
- Li, X-H
- Fan, N
- Lei, D-F
- Wang, Y
- Cai, S-P
- Zhou, X-M
- Chen, X-M
- Liu, X-Y
Producer: 20170417
In:
Genetics and molecular research : GMR vol. 14
Availability: No items available.
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