N. Magnelli

Turner's syndrome and 46,X,i(Yq) karyotype

A. Vianna-Morgante, O. Frota-Pessoa, N. Magnelli, 1974, Journal of medical genetics.

Chromosomal abnormality associated with congenital macroglossia and other

Frota-Pessôa, N. Magnelli, 2022 .

Recessive X‐linked ichthyosis associated with hypertrophic pyloric stenosis: a chance occurrence?

N. Magnelli, L. Bruno, O. Bocanegra, 2003, Clinical and experimental dermatology.

Cytogenetics of 50 patients with mental retardation and multiple congenital anomalies and 50 normal subjects:Madison blind study IV

N. Magnelli, 1976, Clinical genetics.

Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome.

E. Therman, N. Magnelli, 1975, Journal of medical genetics.

Essential tremor, nystagmus and duodenal ulceration: A “new” dominantly inherited condition *

J. Opitz, R. Donaldson, R. Daly, 1976, Clinical genetics.