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Frenny Sheth

Showing results (1-10 of 67) with videos related to

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Molecular Cytogenetics|June 19, 2014
Detection and Inheritance Pattern of Copy Number Variations (CNVs) in Children with Multiple Congenital AnomaliesFrenny Sheth
Indian Journal of Experimental Biology|February 2, 2010
Comparative genomic hybridization array study and its utility in detection of constitutional and acquired anomaliesJoris Andrieux, Frenny Sheth
Indian Pediatrics|February 12, 2013
Diagnostic dilemma in overlapping congenital syndromesFrenny Sheth, Madhumita Kaul
Indian Pediatrics|April 8, 2010
Supernumerary marker chromosome in a child with microcephaly and mental retardationFrenny Sheth, Joris Andrieux, Jayesh Sheth
Indian Pediatrics|July 31, 2002
Prenatal diagnosis of tay-sachs b1 variant in a maharashtrian familyJayesh Sheth, Raktima Bhattacharya, Frenny Sheth
Indian Journal of Pediatrics|May 29, 2007
Ring chromosome 9 in a dysmorphic childJayesh Sheth, Rajesh Joshi, Frenny Sheth
Indian Pediatrics|April 6, 2004
Lysosomal storage disordersJayesh Sheth, Pinaki Patel, Frenny Sheth, et al.
Molecular Cytogenetics|July 24, 2015
Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocationFrenny Sheth, Thomas Liehr, Krati Shah, et al.
International Journal of Dermatology|August 1, 2015
Novel mutation in the XPC gene: a case report of a patient with xeroderma pigmentosumJayesh Sheth, Mehul Mistri, Riddhi Bhavsar, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Novel LINS1 missense mutation in a family with non-syndromic intellectual disabilityJayesh Sheth, Gyan Ranjan, Krati Shah, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Molecular Cytogenetics|June 19, 2014
Detection and Inheritance Pattern of Copy Number Variations (CNVs) in Children with Multiple Congenital AnomaliesFrenny Sheth
Indian Journal of Experimental Biology|February 2, 2010
Comparative genomic hybridization array study and its utility in detection of constitutional and acquired anomaliesJoris Andrieux, Frenny Sheth
Indian Pediatrics|February 12, 2013
Diagnostic dilemma in overlapping congenital syndromesFrenny Sheth, Madhumita Kaul
Indian Pediatrics|April 8, 2010
Supernumerary marker chromosome in a child with microcephaly and mental retardationFrenny Sheth, Joris Andrieux, Jayesh Sheth
Indian Pediatrics|July 31, 2002
Prenatal diagnosis of tay-sachs b1 variant in a maharashtrian familyJayesh Sheth, Raktima Bhattacharya, Frenny Sheth
Indian Journal of Pediatrics|May 29, 2007
Ring chromosome 9 in a dysmorphic childJayesh Sheth, Rajesh Joshi, Frenny Sheth
Indian Pediatrics|April 6, 2004
Lysosomal storage disordersJayesh Sheth, Pinaki Patel, Frenny Sheth, et al.
Molecular Cytogenetics|July 24, 2015
Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocationFrenny Sheth, Thomas Liehr, Krati Shah, et al.
International Journal of Dermatology|August 1, 2015
Novel mutation in the XPC gene: a case report of a patient with xeroderma pigmentosumJayesh Sheth, Mehul Mistri, Riddhi Bhavsar, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Novel LINS1 missense mutation in a family with non-syndromic intellectual disabilityJayesh Sheth, Gyan Ranjan, Krati Shah, et al.
Pageof 7