Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pratima Dash"'
Autor:
Ishwar Chander Verma, Ratna Dua Puri, Meena Lall, Pratima Dash, Udhaya Kotecha, Sunita Bijarnia-Mahay
Publikováno v:
American Journal of Medical Genetics Part A. 170:2119-2126
The utility of fetal autopsy to corroborate antenatal ultrasound findings and to aid genetic counseling is well known. However, the ability to identify an underlying cause for the common indications for which it is performed is not well studied. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb637a65ea7494a34e92cb2914c38a03
https://doi.org/10.1002/ajmg.a.37743
https://doi.org/10.1002/ajmg.a.37743
Autor:
Pratima Dash, Ishwar Chander Verma, Udhaya Kotecha, Ratna Dua Puri, Manisha Goyal, Meena Lall, Sunita Bijarnia
Publikováno v:
Journal of Fetal Medicine. :75-78
Absence or hypoplasia of fetal nasal bone (AHNB) in the first or second trimester scans, with increased risk for trisomy 21 has been shown in many studies. In view of reports of ethnic difference in the size of the nasal bone the usefulness of its ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33f218358d502a0f33cbaf91fb764b83
https://doi.org/10.1007/s40556-015-0051-1
https://doi.org/10.1007/s40556-015-0051-1
Autor:
Ratna Dua Puri, Surbhi Mahajan, Nandita Dimri, Udhaya Kotecha, Ishwar C. Verma, Pratima Dash, Meena Lall, Ashok Baijal, Pushpa Saviour, Preeti Paliwal, Nidhish Sharma, Sunita Bijarnia-Mahay, Swasti Pal
Publikováno v:
Journal of Fetal Medicine. :39-44
Fetal ventriculomegaly (FVM) is a commonly- detected anomaly in the second and third trimester ultrasound scanning. Counseling in this situation is difficult, especially when the chromosomal abnormalities have been excluded. An outcome data would be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::055521fa5c60f55bc20e5178bd39ffe2
https://doi.org/10.1007/s40556-015-0044-0
https://doi.org/10.1007/s40556-015-0044-0
Publikováno v:
Journal of Fetal Medicine. :131-135
The objective of the present study was to analyze the utility of noninvasive prenatal testing (NIPT) for aneuploidies in a developing country like India. NIPT was offered to 500 pregnant women, after review of data of the ongoing pregnancy. Pre-test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4b471ff63e22fdb8a152342179ec85b
https://doi.org/10.1007/s40556-014-0023-x
https://doi.org/10.1007/s40556-014-0023-x
Autor:
Ratna Dua Puri, Udhaya Kotecha, Sunita Bijarnia-Mahay, Meena Lall, Pratima Dash, Ishwar C. Verma
Publikováno v:
Journal of Fetal Medicine. :151-157
Improved antenatal imaging has led to increased detection rates of fetal limb anomalies. While they are nonlethal, they could be the first indication of an underlying genetic disorder. In the event of termination, postmortem and genetic evaluation ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d35c014d3cc6879bf5c29ee0dd169173
https://doi.org/10.1007/s40556-015-0029-z
https://doi.org/10.1007/s40556-015-0029-z
Autor:
Majid Fardaei, Ishwar C. Verma, Rima Slim, Leila Foroughinia, Ngoc Minh Phuong Nguyen, Pratima Dash, Fatemeh Ahmadpour, Maryam Rezaei
Publikováno v:
Human Genome Variation
Recurrent hydatidiform mole (RHM) is defined by the occurrence of repeated molar pregnancies in affected women. Two genes, NLRP7 and KHDC3L, play a causal role in RHM and are responsible for 48–80% and 5% of cases, respectively. Here, we report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d531f316444720c7378bf0d1264db5
https://doi.org/10.1038/hgv.2016.27
https://doi.org/10.1038/hgv.2016.27