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2161.
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2162.
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2163.
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2164.
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2165.
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Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation. [electronic resource] by
- Hannula-Jouppi, Katariina
- Harjama, Liisa
- Einarsdottir, Elisabet
- Elomaa, Outi
- Kettunen, Kaisa
- Saarela, Janna
- Soronen, Minna
- Bouchard, Laura
- Lappalainen, Katriina
- Heikkilä, Hannele
- Kivirikko, Sirpa
- Seppänen, Mikko R J
- Kere, Juha
- Ranki, Annamari
Producer: 20210308
In:
Journal of the American Academy of Dermatology vol. 83
Availability: No items available.
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2166.
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2167.
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2168.
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2169.
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2170.
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2171.
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2172.
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Novel VPS33B mutation in a patient with autosomal recessive keratoderma-ichthyosis-deafness syndrome. [electronic resource] by
- Alter, Svenja
- Hotz, Alrun
- Jahn, Arne
- Di Donato, Nataliya
- Schröck, Evelin
- Smitka, Martin
- von der Hagen, Maja
- Schallner, Jens
- Menschikowski, Mario
- Gillitzer, Claus
- Laass, Martin W
- Fischer, Judith
- Tzschach, Andreas
Producer: 20191029
In:
American journal of medical genetics. Part A vol. 176
Availability: No items available.
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2173.
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2174.
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2175.
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2176.
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2177.
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2178.
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2179.
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2180.
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