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A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics. [electronic resource] by
- Schreyer-Shafir, Nira
- Huizing, Marjan
- Anikster, Yair
- Nusinker, Ziva
- Bejarano-Achache, Idit
- Maftzir, Genia
- Resnik, Luba
- Helip-Wooley, Amanda
- Westbroek, Wendy
- Gradstein, Libe
- Rosenmann, Ada
- Blumenfeld, Anat
Producer: 20061207
In:
Human mutation vol. 27
Availability: No items available.
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Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy. [electronic resource] by
- Zelinger, Lina
- Cideciyan, Artur V
- Kohl, Susanne
- Schwartz, Sharon B
- Rosenmann, Ada
- Eli, Dalia
- Sumaroka, Alexander
- Roman, Alejandro J
- Luo, Xunda
- Brown, Cassondra
- Rosin, Boris
- Blumenfeld, Anat
- Wissinger, Bernd
- Jacobson, Samuel G
- Banin, Eyal
- Sharon, Dror
Producer: 20150716
In:
Ophthalmology vol. 122
Availability: No items available.
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