Preimplantation genetic diagnosis of chromosomal abnormalities by multicolour fluorescence in situ hybridisation.

Parikh, F R; Madon, P F; Athalye, A S; Naik, N J; Gada, S D; Ganla, K N; Nadkarni, S G; Patki, A S; Khot, S S

Parikh, F R; Madon, P F; Athalye, A S; Naik, N J; Gada, S D; Ganla, K N; Nadkarni, S G; Patki, A S; Khot, S S.

Affiliation

Parikh FR; Department of Assisted Reproduction and Genetics, Jaslok Hospital and Research Center, Mumbai.

J Indian Med Assoc ; 99(8): 441-4, 2001 Aug.

Article in En | MEDLINE | ID: mdl-11881859

Subject(s)

Genetic Testing/methods; In Situ Hybridization, Fluorescence; Preimplantation Diagnosis/methods; Blastomeres; Chromosome Aberrations; Embryo Transfer; Female; Fertilization in Vitro/methods; Humans; Pregnancy; Prospective Studies; Sensitivity and Specificity

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Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / In Situ Hybridization, Fluorescence / Preimplantation Diagnosis Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies / Screening_studies Limits: Female / Humans / Pregnancy Language: En Journal: J Indian Med Assoc Year: 2001 Document type: Article Country of publication: India

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