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Journal of Clinical and Experimental Genetics (JCEG) is an open access, peer reviewed multidisciplinary refereed journal devoted to the rapid publication of fundamental advances and innovative research works in the field of Clinical and Experimental genetics by making it freely accessible by various researchers and academicians.

Journal of Clinical and Experimental Genetics is using online manuscript submission, review and tracking systems for quality and quick review processing. Review processing is performed by the editorial board members of Journal of Clinical and Experimental Genetics or outside experts; at least two independent reviewer's approval followed by editor approval is required for acceptance of any citable manuscript.

Archives

Vol-04 | Issue-1-2024

The Opinions of Medical Faculty Students on the Levels of Genetic Knowledge

The aim of this study is to determine the basic genetic knowledge of medical school students and their self-reported knowledge about some genetic defects-diseases and genetic counseling

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Smoking and Male Infertility ׃ A comprehensive Review

Infertility is a serious concern affecting millions of couples globally. Natural conception is seen to be achieved in 80-85% couples leading 15 % couples suffer worldwide.

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Identification of Novel De-Novo 12q14 -12q22 Gene Mutations and MTHFR C677T Gene Polymorphism Increase Genetic Susceptibility in Hirschsprung Disease - A Rare Case Report

Clinically diagnosed male proband shows typical Mongolian type features like flat broad nasal septum with protruded tongue and broad forehead with epicanthal folding.

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Bagatelle Cassidy Syndrome: Macrocephaly with Fronto-Facial Dysmorphism and Hearing Loss; an Extremely Rare Case

Bagatelle Cassidy syndrome is a very rare disease first described in 1995 in a boy with macrocephaly, hypertelorism, hearing loss, developmental delay and facial dysmorphism

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Low RNA Binding Strength of Human X Chromosome may contribute to X Chromosome Inactivation

During early embryonic development in female mammals, one copy of the X Chromosome is randomaly

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    NIKOLAI N. MODYANOV

    Professor, Department of Physiology and Pharmacology, The University of Toledo College of Medicine, United States

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    CHARLES WANG

    Professor, Director Center for Genomics School of Medicine, Loma Linda University, United States

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    ERIC HUANG

    Professor, Division of Dermatology, University of California, United States

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    NICHOLAS TSINOREMAS

    Research Professor, Department of Medicine, University of Miami, United States

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    MASAYOSHI YAMAGUCHI

    Adjunct Professor, Department of Hematology and Biomedical Oncology, Emory University School of Medicine, United States

Recent Articles

The Opinions of Medical Faculty Students on the Levels of Genetic Knowledge

The aim of this study is to determine the basic genetic knowledge of medical school students and their self-reported knowledge about some genetic defects-diseases and genetic counseling

Author Name: Bilgin Kıray Vural
PDF | Full Text | Journal of Clinical and Experimental Genetics
Smoking and Male Infertility: A Comprehensive Review

Infertility is a serious concern affecting millions of couples globally. Natural conception is seen to be achieved in 80-85% couples leading 15 % couples suffer worldwide

Author Name: Hameed Mahrukh
PDF | Full Text | Journal of Clinical and Experimental Genetics
Identification of Novel De-Novo 12q14 -12q22 Gene Mutations and MTHFR C677T Gene Polymorphism Increase Genetic Susceptibility in Hirschsprung Disease - A Rare Case Report

Hirschsprung's disease (HSCR) is a complex congenital genetic aganglionic disorder of intestine fall under paediatric age group of “Birth Defects”.

Author Name: Saxena Ajit K
PDF | Full Text | Journal of Clinical and Experimental Genetics
Bagatelle Cassidy Syndrome: Macrocephaly with Fronto-Facial Dysmorphism and Hearing Loss; an Extremely Rare Case

Bagatelle Cassidy syndrome is a very rare disease first described in 1995 in a boy with macrocephaly, hypertelorism, hearing loss, developmental delay and facial dysmorphism. The cause of this syndrome is unknown and has no specific diagnostic test. W

Author Name: Avina Fierro JA
PDF | Full Text | Journal of Clinical and Experimental Genetics