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1001.
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1002.
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1003.
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1004.
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1005.
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1006.
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1007.
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AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout-NLS-lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue-specificity. [electronic resource] by
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- Hu, Yuanyuan
- Smith, Charles E
- Richardson, Amelia S
- Zhang, Hong
- Yang, Jie
- Lin, Brent
- Wang, Shih-Kai
- Kim, Jung-Wook
- Chun, Yong-Hee
- Simmer, James P
- Hu, Jan C-C
Producer: 20200617
In:
Molecular genetics & genomic medicine vol. 7
Availability: No items available.
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1008.
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1009.
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1010.
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1011.
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1012.
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1013.
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1014.
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Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes. [electronic resource] by
- Pêgo, Sabina Pena B
- Coletta, Ricardo D
- Dumitriu, Simona
- Iancu, Daniela
- Albanyan, Saleh
- Kleta, Robert
- Auricchio, Maria Teresa
- Santos, Luis Antônio
- Rocha, Breno
- Martelli-Júnior, Hercílio
Producer: 20170918
In:
Oral surgery, oral medicine, oral pathology and oral radiology vol. 123
Availability: No items available.
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1017.
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Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations. [electronic resource] by
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- Kang, J
- Kim, Y J
- Seymen, F
- Kasimoglu, Y
- Lee, Z H
- Shin, T J
- Hyun, H K
- Kim, Y J
- Lee, S H
- Hu, J C C
- Simmer, J P
- Kim, J W
Producer: 20190909
In:
Journal of dental research vol. 97
Availability: No items available.
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1018.
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1019.
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1020.
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