Trisomy 21 q: 46,XX,21s+/47,XX,+21q−(q22→qter) mosaicism (de novo) in a down syndrome child

Author:

Murthy D. S. Krishna,Roy Sabita,Contractor P. M.,Shah V. C.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Lejeune J, Gautier M, Turpin R: Etude des chromosomes somatiques de neuf enfants mongoliens.Compt Rend 248: 1721, 1959

2. Borgaonkar DS:Chromosomal variation in man. A catalog of chromosomal variants and anomalies. 3rd Edition, Alan R Liss, Inc New York, 1980, p 391

3. Mikkelsen M: Down's syndrome: current stage of cytogenetic research.Humangenetics, 12: 1, 1971

4. Krishna Murthy DS, Patel ZM, Ambani LM: Trisomy 18 q: 46,XX, 13q+,t(13;18) (q32;q11) in a new born associated with multiple congenital annomalies due to paternal reciprocal translocation, 46,XX,−13,+der(13),t(13;18)(q321q11).Clin Genet 18: 233, 1980

5. Sinet PM, Conturier J, Dutrillaux B: Trisomie 21 et superoxide dismutate −1 (IPO-A). Tentative de localisation sur la sons bande 21q22.1.Expt Cell Res 97: 47, 1976

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