Fortunato Lonardo
0000-0002-5712-0754
48 papers found
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"A Case of Autosomal Recessive Form of Cranio-Metaphyseal Dysplasia with Unusual Features and with Bone Fragility"
Two sibs affected by Pendred's syndrome in a family with recurrent goiter.
Cytogenetic study of a cell line of human penile cancer.
[Poland-Moebius syndrome. Description of a new case]
Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
Prenatal diagnosis of Mohr syndrome by ultrasonography
Gastroschisis in two sibs with abdominal hernia in maternal grandfather and greatgrandfather
[Phenotype anomalies in subjects with balanced chromosome translocation. Presentation of 4 cases]
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