Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis

We reviewed the distribution of autosomal fragile sites (FS) and spontaneous chromosome breaks or gaps (CB) at chromosome locations other than those recognized as FS from 100 amniotic fluid samples (AF), 19 chorionic villus samples (CVS), and 5 percutaneous umbilical blood samples (PUBS) referred fo...

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Veröffentlicht in:	American journal of medical genetics 1991-02, Vol.38 (2-3), p.456-463
Hauptverfasser:	Krawczun, Michael S., Jenkins, Edmund C., Duncan, Charlotte J., Stark-Houck, Sandra L., Kunaporn, Suphat, Schwartz-Richstein, Carol, Gu, Hong, Brown, W. Ted
Format:	Artikel
Sprache:	eng
Schlagworte:	Amniotic Fluid - cytology autosomal fragility Biological and medical sciences Cells, Cultured Chorionic Villi - ultrastructure Chromosome Fragile Sites Chromosome Fragility Female Fetal Blood - cytology Fragile X Syndrome - diagnosis Fragile X Syndrome - pathology fragile(X)(q27) Humans Lymphocytes - ultrastructure Male Medical genetics Medical sciences Pregnancy Prenatal Diagnosis
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