WFRF:(Treadwell M)
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Mutational spectrum of NSDHL in CHILD syndrome.
- Bornholdt, D (author)
- König, A (author)
- Happle, R (author)
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- Leveleki, L (author)
- Bittar, M (author)
- Danarti, R (author)
- Tilgen, W (author)
- Reinhold, U (author)
- Poiares Baptista, A (author)
- Grosshans, E (author)
- Vabres, P (author)
- Niiyama, S (author)
- Sasaoka, K (author)
- Tanaka, T (author)
- Maiss, AL (author)
- Treadwell, PA (author)
- Lambert, D (author)
- Camacho, F (author)
- Grzeschik, KH (author)
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- (creator_code:org_t)
- BMJ, 2005
- 2005
- English.
- In: J Med Genet. - : BMJ. ; 42, s. 1-6
- Journal article (pop. science, debate, etc.)
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- art (subject category)
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- Bornholdt, D
- König, A
- Happle, R
- Leveleki, L
- Bittar, M
- Danarti, R
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- Vahlquist, Ander ...
- Tilgen, W
- Reinhold, U
- Poiares Baptista ...
- Grosshans, E
- Vabres, P
- Niiyama, S
- Sasaoka, K
- Tanaka, T
- Maiss, AL
- Treadwell, PA
- Lambert, D
- Camacho, F
- Grzeschik, KH
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- Articles in the publication
- J Med Genet
- Journal of Medic ...
- By the university
- Uppsala University
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