Biomedical subjects
R R GORDON
Publications and source records attributed to R R GORDON.
"CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY.
Explore the source record for details and available documents.
MENINGEAL INFECTIONS IN CHILDHOOD.
Explore the source record for details and available documents.
RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISM.
Explore the source record for details and available documents.
HAEMOPHAGOCYTIC RETICULOSIS DIAGNOSED DURING LIFE.
Explore the source record for details and available documents.
Ambiguous sex in the newborn.
Explore the source record for details and available documents.
Neonatal cold injury and hypothyroidism.
Explore the source record for details and available documents.
Congenital hypoplastic anaemia (pure red-cell anaemia) with periodic erythroblastopenia.
Explore the source record for details and available documents.
Social status of the parents of cerebral palsied children.
Explore the source record for details and available documents.
Rh antibody titres and foetal wastage.
Explore the source record for details and available documents.
Chromosome count in a hermaphrodite with some features of Klinefelter's syndrome.
Explore the source record for details and available documents.
Periodic pyrexia and erythema multiforme.
Explore the source record for details and available documents.
Extended exchange transfusion in pre-hydropic infants.
Explore the source record for details and available documents.
Congenital amegakaryocytic thrombocytopenia with congenital deformities and a leukemoid blood picture in the newborn.
Explore the source record for details and available documents.
Persistence of foetal periderm and Zenker's degeneration of muscle in a full-term infant.
Explore the source record for details and available documents.