Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Bhairi, Vidya"'
Publikováno v:
Journal of Fetal Medicine; Dec2021, Vol. 8 Issue 4, p311-314, 4p
Publikováno v:
International Journal of Molecular and Cellular Medicine
We present 2 cases of likely rare event. In case 1, 3rd degree consanguineous marriage revealed inv(6) with same break points in parents who were found to be phenotypically normal. The same inv(6) being inherited in progeny but presented with low AMH
Autor:
Jadhav A; Clinical Cytogenetics Department, Lilac Insights Pvt. Ltd., Navi Mumbai, (Maharashtra), India., Jadhav Y; Clinical Cytogenetics Department, Lilac Insights Pvt. Ltd., Navi Mumbai, (Maharashtra), India., Bhairi V; Clinical Cytogenetics Department, Lilac Insights Pvt. Ltd., Navi Mumbai, (Maharashtra), India., Ansari R; Clinical Cytogenetics Department, Lilac Insights Pvt. Ltd., Navi Mumbai, (Maharashtra), India., Torane P; Clinical Cytogenetics Department, Lilac Insights Pvt. Ltd., Navi Mumbai, (Maharashtra), India., Patil K; Clinical Cytogenetics Department, Lilac Insights Pvt. Ltd., Navi Mumbai, (Maharashtra), India.
Publikováno v:
International journal of molecular and cellular medicine [Int J Mol Cell Med] 2023; Vol. 12 (1), pp. 81-85.