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Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited condition.
Clin Genet. 1976 Jan;9(1):81-91. doi: 10.1111/j.1399-0004.1976.tb01553.x.
Clin Genet. 1976.
PMID: 1248168
Cytogenetics of 50 patients with mental retardation and multiple congenital anomalies and 50 normal subjects. Madison blind study IV.
Magnelli NC.
Magnelli NC.
Clin Genet. 1976 Feb;9(2):169-82. doi: 10.1111/j.1399-0004.1976.tb01564.x.
Clin Genet. 1976.
PMID: 1248176
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Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome.
Magnelli NC, Therman E.
Magnelli NC, et al.
J Med Genet. 1975 Mar;12(1):105-8. doi: 10.1136/jmg.12.1.105.
J Med Genet. 1975.
PMID: 1121016
Free PMC article.
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Turner's syndrome and 46,X,i(Yq) karyotype.
Magnelli NC, Vianna-Morgante AM, Frota-Pessoa O, Taboada-Lopez MG.
Magnelli NC, et al.
J Med Genet. 1974 Dec;11(4):403-6. doi: 10.1136/jmg.11.4.403.
J Med Genet. 1974.
PMID: 4443992
Free PMC article.
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[INCIDENCE OF DIABETES MELLITUS IN ARTERIOSCLEROTICS OLDER THAN 55 YEARS].
ARRIGONI HE, SURIS MJ, DEALVAREZ HT, MAGNELLI NC, BUSTOS LA, COLQUE CM, SHOCRON S, ANGELA M, DOLONGUEVICH B, ESPINOSA E, CAMPANA H, DIBENEDETTO H.
ARRIGONI HE, et al. Among authors: magnelli nc.
Dia Med. 1964 Mar 19;36:181.
Dia Med. 1964.
PMID: 14147852
Spanish.
No abstract available.
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