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Page 1
Mutational spectrum of NSDHL in CHILD syndrome.
Bornholdt D, König A, Happle R, Leveleki L, Bittar M, Danarti R, Vahlquist A, Tilgen W, Reinhold U, Poiares Baptista A, Grosshans E, Vabres P, Niiyama S, Sasaoka K, Tanaka T, Meiss AL, Treadwell PA, Lambert D, Camacho F, Grzeschik KH. Bornholdt D, et al. Among authors: grosshans e. J Med Genet. 2005 Feb;42(2):e17. doi: 10.1136/jmg.2004.024448. J Med Genet. 2005. PMID: 15689440 Free PMC article. No abstract available.
[Atrophic chronic polychondritis].
Brehm K, Grosshans E, Happle R. Brehm K, et al. Among authors: grosshans e. Rev Clin Esp. 1970 Jun 30;117(6):567-72. Rev Clin Esp. 1970. PMID: 5518940 Spanish. No abstract available.
[Chronic atrophic polychondritis].
Brehm K, Grosshans E, Happle R. Brehm K, et al. Among authors: grosshans e. Cah Med. 1970 Jul;11(9):795-801. Cah Med. 1970. PMID: 5453262 French. No abstract available.
[Polychondritis chronica atrophicans].
Brehm K, Grosshans E, Happle R. Brehm K, et al. Among authors: grosshans e. Minerva Med. 1970 Sep 12;61(73):3856-62. Minerva Med. 1970. PMID: 5454453 Italian. No abstract available.
[Chronic atrophic polychondritis].
Brehm K, Grosshans E, Happle R. Brehm K, et al. Among authors: grosshans e. Munch Med Wochenschr. 1970 Jun 19;112(25):1200-5. Munch Med Wochenschr. 1970. PMID: 5467935 German. No abstract available.
481 results