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F Sheth

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Articles 5
Citations 18
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Recent Articles
1.
Thuresson A, Van Buggenhout G, Sheth F, Kamate M, Andrieux J, Clayton Smith J, et al.
Clin Genet . 2016 May; 91(1):106-110. PMID: 27153334
Duplications at 2q24.3 encompassing the voltage-gated sodium channel gene cluster are associated with early onset epilepsy. All cases described in the literature have presented in addition with different degrees of...
2.
Sheth H, Sheth J, Sheth F, Burn J
Diabet Med . 2015 Jun; 33(1):134-5. PMID: 26053687
No abstract available.
3.
Sheth F, Akinde O, Datar C, Adeteye O, Sheth J
Case Rep Genet . 2012 Dec; 2012:878796. PMID: 23227376
The Wolf-Hirschhorn syndrome (WHS) is a multiple malformation and contiguous gene syndrome resulting from the deletion encompassing a 4p16.3 region. A microscopically visible terminal deletion on chromosome 4p (4p16→pter) was...
4.
Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Patil S, et al.
Cytogenet Genome Res . 2009 Sep; 125(2):115-6. PMID: 19729914
Here we report the first case of an inverted duplicated neocentric small supernumerary marker chromosome present in a karyotype 47,XX,+mar(Y). As expected a partial disomy of Ypter to Yp11.2 did...
5.
Sheth J, Thakore P, Shah S, Shah B, Shan N, Sheth F
J Assoc Physicians India . 1989 Nov; 37(11):703-4. PMID: 2632535
Attempt has been made to rationalise the biochemical assessment of patients suspected to have thyroid dysfunction by introduction of a new rapid and supersensitive immunoradiometric assay (IRMA) for TSH. 294...