Similar articles

• A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+).

  Yanagisawa S. Yanagisawa S. Jinrui Idengaku Zasshi. 1972 Sep;17(1):38-43. Jinrui Idengaku Zasshi. 1972. PMID: 4265909 No abstract available.
• [Partial trisomy for the segment 21(q11----qter) resulting from a de novo translocation between chromosomes 5 and 21].

  Crippa L, Ballaman J, Engel E. Crippa L, et al. Ann Genet. 1984;27(3):190-3. Ann Genet. 1984. PMID: 6239590 French.
• [The autosomal chromosome aberrations in ophthalmology].

  François J. François J. J Genet Hum. 1966;15:Suppl:133-208. J Genet Hum. 1966. PMID: 4873685 Review. French. No abstract available.
• [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].

  Fioretti G, Pagano L, Renda S, Festa B, Rinaldi A, Celona A, Casullo C, Stabile M, Cavaliere ML, Ventruto V. Fioretti G, et al. Minerva Pediatr. 1980 Jun 30;32(12):807-14. Minerva Pediatr. 1980. PMID: 7464734 Italian. No abstract available.
• Autosomal chromosome aberrations in ophthalmology.

  Francois J. Francois J. Int Ophthalmol Clin. 1968 Winter;8(4):839-910. Int Ophthalmol Clin. 1968. PMID: 4244691 Review. No abstract available.