Omphalocele and partial trisomy 1q syndrome-Reference-Cited by-同舟云学术

Omphalocele and partial trisomy 1q syndrome

Published:1979 Issue:1 Volume:53 Page:1-4
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Chen H.,Gershanik J. J.,Mailhes J. B.,Sanusi I. D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00289442.pdf

Reference27 articles.

1. Boué, J. G., Boué, A.: Fréquence des aberrations chromosomiques dans les avorterments spontanés humains. C. R. Acad. Sci. [D] (Paris) 269, 283?286 (1969)

2. Colombani, P. M., Cunningham, D.: Perinatal aspects of omphalocele and gastroschisis. Am. J. Dis. Child. 131, 1386?1388 (1977)

3. Eriksson, B., Fraccaro, M., Hulten, M., Lindsten, J., Thoren, C., Tiepolo, L.: Structural abnormalities of chromosome 18. II. Two familial translocation, B/18 and 16/18, ascertained through unbalanced forms. Ann. Genet. 14, 281?290 (1971)

4. Finley, W. H., Garrett, J. H., Finley, S. C.: Partial trisomy 1q. Am. J. Hum. Genet. 27, 35A (1975)

5. Garrett, J. H., Finley S. C., Finley, W. H.: Fetal loss and familial chromosome 1 translocations. Clin. Genet. 8, 341?348 (1975)

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