References
Relief AE, Van Zyl JA, Menkveld R et al. Chromosome studies in 496 infertile males with a sperm count below 10 million.Hum Genet: 1984; 66 : 162–167.
Qazi QH, Kassner EG, Masakawa A et al. The SC phocomelia syndrome.Am J Med Genet 1979; 4: 231–238.
Schwartz S, Palmer C. Chromosomal findings in 164 couples with repeated spontaneous abortions: With special consideration to prior reproductive history.Hum Genet 1983; 63 : 28–34.
Dodson MG. New concepts and questions in gestational trophoblastic disease.J Reprod Med 1983; 28: 741–749.
Ferguson-Smith MA, Yates JRW. Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative European study on 52,965 amniocentesis.Prenat Diagn (Special Issue) 1984; 4 : 5–44.
Stene J, Stene E, Mikkelsen M. Risk for chromosome abnormality at amniocentesis, following a child with a noninherited chromosome aberration.Prenat Diagn (Special Issue) 1984; 4: 81–95.
Boue’ A, Gallano. P. A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.Prenat Diagn (Special Issue) 1984; 4: 45–67.
Jenkins EC, Brown WT, Wilson MG, et al. The prenatal detection of the fragile X chromosome: Review of a recent experience.Am J Med Genet 1986; 23 : 297–312.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Qazi, Q.H. Indications for cytogenetic studies. Indian J Pediatr 56, 454–457 (1989). https://doi.org/10.1007/BF02722412
Issue Date:
DOI: https://doi.org/10.1007/BF02722412