A Probable 17-18 Trisomy Syndrome with Phocomelia, Exomphalos, and Agenesis of Hemidiaphragm

Author:

Kajii T.,Oikawa K.,Itakura K.,Ohsawa T.

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Chromosome studies in abortuses and stillborn infants;H, Carr D.;Lancet,1963

2. A new trisomic syndrome;M.., Edwards. J. H.. Harnden. D. G.. Cameron. A. H.. Crosse V.; Wolff, 0. H,1960

3. Autosomal trisomy of a group 16-18 chromosome;Germ-an. J. L.. 111. Rankin. J. K.. Harrison. P. A.. Donovan. D. J., Hogan. W. J.; G, Bearn. A.;J. Pediat,1962

4. Trisomy-17 syndrome. Report of three cases and review of the literature;Hirschhorn, Gottlieb M.I.; Cooper, K.; Moloshok, H.L.Lusskin N.; E.., R.; L, Hodes H.;Amer. J. Med,1962

5. The No. 17-18 (E) trisomy syndrome;S., Hecht F.Bryant J.; G.., Motulsky A.; Giblett, E.R.;J. Pediat,1963

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2. Congenital Diaphragmatic Hernia;Sabiston and Spencer's Surgery of the Chest;2010

3. Four cases of trisomy 18 syndrome with limb reduction malformations.;Journal of Medical Genetics;1984-08-01

4. Schisis-association;American Journal of Medical Genetics;1981

5. Omphalocele and partial trisomy 1q syndrome;Human Genetics;1979

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