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Mutations in the gene LEMD3 in...
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Stalna poveznica
Mutations in the gene LEMD3 in patients with osteopoikilosis and melorheostosis - Evidence for genetic heterogeneity
Bibliografski detalji
Glavni autori:
Couto, A
,
Armas, J
,
Brown, M
,
Peach, C
,
Wordsworth, P
,
Zhang, Y
Format:
Conference item
Izdano:
2006
Primjerci
Opis
Slični predmeti
Prikaz za djelatnike knjižnice
Slični predmeti
A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis.
od: Couto, A, i dr.
Izdano: (2007)
Novel and recurrent germline LEMD3 mutations causing Buschke-Ollendorff syndrome and osteopoikilosis but not isolated melorheostosis.
od: Zhang, Y, i dr.
Izdano: (2009)
A novel LEMD3 pathogenic variant in a son and mother with osteopoikilosis
od: Selin Elmaoğulları, i dr.
Izdano: (2019-08-01)
Osteopoikilosis and multiple exostoses caused by novel mutations in <it>LEMD3 </it>and <it>EXT1 </it>genes respectively - coincidence within one family
od: Horn Denise, i dr.
Izdano: (2010-07-01)
Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant
od: Benjamin Korman, i dr.
Izdano: (2016-01-01)