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1 research outputs found
A cytogenetic deletion, del(17)(q11.22q21.1), in a patient with sporadic neurofibromatosis type 1 (NF1) associated with dysmorphism and developmental delay.
Author
A O Wilkie
Barker D.
+39Â more
Cawthon R.M.
Chomczynski P.
E Sorour
Golgar D.E.
Grimm T.
H E Hughes
Huson S.M.
Huson S.M.
J Maynard
Jadayel D.
Kayes L.M.
Kayes L.M.
Ketterling R.P.
Korf B.
Lazaro C.
M Upadhyaya
M Vaughan
Marchuk D.A.
Morton N.E.
Neitzel H.
P W Thompson
Purandare S.M.
Rodenhiser D.
S H Roberts
Schmickel R.D.
Seabright M.
Seizinger B.R.
Shimmin L.C.
Stephans K.
Tint G.S.
Upadhyaya M.
Upadhyaya M.
Upadhyaya M.
Upadhyaya M.
Upadhyaya M.
Viskochil D.H.
Wallace M.R.
Wheater R.F.
Xu G.
Publication venue
'BMJ'
Publication date
Field of study
No full text
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