12 results on '"Giraud, F."'
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2. Abnormal Childhood Phenotypes Associated with the Same “Balanced” Chromosome Rearrangements as In the Parents
3. Origin of the Supernumerary Chromosome in Trisomy 21
4. X-linked mental retardation, growth retardation, deafness and micro-genitalism. A second familial report.
5. Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1.
6. Dermatoglyphics in parents of children with trisomy 21.
7. Fryns syndrome: report on 8 new cases.
8. Spontaneous Chromosome Breaks in Vitro
9. Origin of the Supernumerary Chromosome in Trisomy 21.
10. Abnormal Childhood Phenotypes Associated with the Same 'Balanced' Chromosome Rearrangements as In the Parents.
11. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.
12. Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion.
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