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Mutations in the gene LEMD3 in...
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Easpórtáil chuig EndNote
Buan-nasc
Mutations in the gene LEMD3 in patients with osteopoikilosis and melorheostosis - Evidence for genetic heterogeneity
Sonraí bibleagrafaíochta
Príomhchruthaitheoirí:
Couto, A
,
Armas, J
,
Brown, M
,
Peach, C
,
Wordsworth, P
,
Zhang, Y
Formáid:
Conference item
Foilsithe / Cruthaithe:
2006
Stoc
Cur síos
Míreanna comhchosúla
Amharc foirne
Míreanna comhchosúla
A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis.
de réir: Couto, A, et al.
Foilsithe / Cruthaithe: (2007)
Novel and recurrent germline LEMD3 mutations causing Buschke-Ollendorff syndrome and osteopoikilosis but not isolated melorheostosis.
de réir: Zhang, Y, et al.
Foilsithe / Cruthaithe: (2009)
A novel LEMD3 pathogenic variant in a son and mother with osteopoikilosis
de réir: Selin Elmaoğulları, et al.
Foilsithe / Cruthaithe: (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
de réir: Horn Denise, et al.
Foilsithe / Cruthaithe: (2010-07-01)
Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant
de réir: Benjamin Korman, et al.
Foilsithe / Cruthaithe: (2016-01-01)