Mosaic Trisomy 1q Due to a De Novo Translocation in a Foetus With Early Developmental Abnormalities (Karyotype 46,XY,der(14),t(1;14)(p11;p11.2)/46,xy) Delineation of Parent and Cell Stage of Origin

International Journal of Human Genetics - India
doi 10.31901/24566330.2008/08.04.01
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Genetics
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Kamla Raj Enterprises

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