Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype

Author:

Aguinaga M.,Razo G.,Castro J.,Mayén-Molina D. G.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference17 articles.

1. A case of apparent trisomy 21 without the Down's syndrome phenotype.

2. 1991. Amniotic Fluid I: Flask culture, harvesting and staining. Protocols and Peripheral Blood Culture. In The ACT Cytogenetics Laboratory Manual. The Association of Cytogenetic Technologist (2nd edn), (ed.). Raven Press: New York; 17–23, 172–181.

3. Prenatal diagnosis of partial monosomy 18p(18p11.2?pter) and trisomy 21q(21q22.3?qter) with alobar holoprosencephaly and premaxillary agenesis

4. Cryptic duplication of 21q in an individual with a clinical diagnosis of Down syndrome

5. . 2004. Autosomal reciprocal translocations. In Chromosome Abnormalities and Genetic Counseling (3rd edn), (eds). Oxford University Press: New York; 79–83.

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