论文信息 - Trisomy 20 mosaicism in amniotic fluid cell culture

Trisomy 20 mosaicism in amniotic fluid cell culture

Chromosomal mosaicism in cultured amniotic fluid cells presents one of the most difficult problems in prenatal diagnosis in predicting the foetal phenotype. We present a case in which trisomy 20 mosaicism was diagnosed prenatally but not confirmed in the aborted foetus.

N. Nevin | W. Thompson | J. Nevin

[1] M. Ryynänen,et al. Incomplete prenatal diagnosis of G‐trisomy mosaicism , 1978, Clinical Genetics.

[2] D. Luthy,et al. Amniotic fluid cell mosaicism for presumptive trisomy 20 , 1978, Clinical genetics.

[3] U. Francke,et al. Familial trisomy 20p five cases and two carriers in three generations a review. , 1977, Annales de genetique.

[4] E. Jenkins,et al. Chromosomal mosaicism in amniotic fluid cell cultures. , 1977, The Journal of pediatrics.

[5] K. Hirschhorn,et al. Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant , 1976 .

[6] D. Harnden,et al. TRISOMY-20 SYNDROME IN MAN , 1976, The Lancet.

[7] J. Opitz,et al. TRISOMY-20 SYNDROME IN MAN , 1976, The Lancet.

[8] M. Kaback,et al. Chromosomal mosaicism in amniotic cell culture. A diagnostic Dilemma. , 1975, Israel journal of medical sciences.

[9] Rudd Nl,et al. Mosaicism in amniotic fluid cell cultures. , 1977 .

[10] R. Worton,et al. Mosaicism in amniotic fluid cell cultures. , 1977, Birth defects original article series.