10 results on '"Ter Haar B"'
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2. Studies on hair roots for carrier detection in hypoxanthine‐guanine phosphoribosyl transferase deficiency
3. Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs.
4. The Nathalie syndrome. A new hereditary syndrome.
5. Orbital cyst in addition to congenital cerebral and focal dermal malformations: a new entity.
6. Studies on hair roots for carrier detection in hypoxanthine-quanine phosphoribosyl transferase deficiency.
7. Trisomy for the short arm of chromosome No. 10.
8. Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletion.
9. Bloom's syndrome in two Dutch families.
10. 2:2 and 3:1 meiotic disjunctions in a carrier of a reciprocal 10/14 translocation.
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