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pro vyhledávání: '"Rahim Gholipoorfeshkecheh"'
Autor:
Rahim Gholipoorfeshkecheh, Swati Agarwala, Kavya G, Santhosh Krishnappa, Mysore R. Savitha, Nallur B. Ramachandra
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background Homozygosity mapping is an efficient gene mapping method applicable to recessive disorders. It can detect homozygous segments of identical haplotype structures shared at a higher frequency among ventricular septal defect (VSD) and
Externí odkaz:
https://doaj.org/article/7d0add788ac04f9487605ac060d6e936
Autor:
Mysore R. Savitha, Santhosh Krishnappa, Swati Agarwala, Kavya G, Rahim Gholipoorfeshkecheh, Nallur B. Ramachandra
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Background Homozygosity mapping is an efficient gene mapping method applicable to recessive disorders. It can detect homozygous segments of identical haplotype structures shared at a higher frequency among ventricular septal defect (VSD) and tetralog
Autor:
Mysore R. Savitha, Santhosh Krishnappa, Nallur B. Ramachandra, Swati Agarwala, Rahim Gholipoorfeshkecheh, Doddaiah Narayanappa
Publikováno v:
Gene Reports. 19:100613
Cardiogenesis starts at around the third week of gestation and require precise gene signalling through various transcription factors. Irregularities in gene signalling lead to various types of Congenital Heart Diseases (CHDs). Since the Ventricular S