Home

Select data courtesy of the U.S. National Library of Medicine.

Home

Molecular Genetics & Genomic Medicine | DeepDyve

Molecular Genetics & Genomic Medicine

Subject:: Genetics
Publisher:: Wiley Subscription Services, Inc., A Wiley Company — Wiley
ISSN:
Scimago Journal Rank:: 34

2026

Volume 14

Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2025

Volume 13

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)

2024

Volume 12

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2023

Volume 11

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2022

Volume 10

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2021

Volume 9

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2020

Volume 8

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2019

Volume 7

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2018

Volume 6

Issue 6 (Jan)Issue 5 (Jan)Issue 4 (Jan)Issue 3 (Jan)Issue 2 (Jan)Issue 1 (Jan)

2017

Volume 5

Issue 6 (Jan)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2016

Volume 4

Issue 6 (Nov)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2015

Volume 3

Issue 6 (Nov)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2014

Volume 2

Issue 6 (Nov)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2013

Volume 1

Issue 4 (Nov)Issue 3 (Sep)Issue 2 (Jul)Issue 1 (May)

journal article

Open Access Collection

Association of MACROD2 gene variants with obesity and physical activity in a Korean population

Kim, Hye‐Rim; Jin, Hyun‐Seok; Eom, Yong‐Bin

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1635pmid: 33624934

journal article

Open Access Collection

Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis

Xie, Fei; Lei, Lei; Cai, Bin; Gan, Lu; Gao, Yu; Liu, Xiaoying; Zhou, Lin; Jiang, Jinjin

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1577pmid: 33620149

journal article

Open Access Collection

First reported CABP2‐related non‐syndromic hearing loss in Northern Europe

Sheyanth, Inger Norlyk; Højland, Allan Thomas; Okkels, Henrik; Lolas, Ihab; Thorup, Christian; Petersen, Michael Bjørn

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1639pmid: 33666369

journal article

Open Access Collection

High throughput screening for expanded CTG repeats in myotonic dystrophy type 1 using melt curve analysis

Butterfield, Russell J.; Imburgia, Carina; Mayne, Katie; Newcomb, Tara; Dunn, Diane M.; Duval, Brett; Feldkamp, Marcia L.; Johnson, Nicholas E.; Weiss, Robert B.

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1619pmid: 33624941

journal article

Open Access Collection

Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam

Nghiem, Trung Dung; Do, Gia Tuyen; Luong, Long Hoang; Nguyen, Quy Linh; Dang, Ha Viet; Viet, Anh Nguyen; Nguyen, Thuy Thu; Tran, Van Khanh; Ta, Thanh Van; Tran, Thinh Huy

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1648pmid: 33687153

journal article

Open Access Collection

Mutation analysis and prenatal diagnosis of a family with congenital contractural arachnodactyly

Hu, Lin; Li, Huanzheng; Sun, Guang; Wu, Ke; Luan, Zhaotang; Xiang, Yanbao; Tang, Shaohua

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1638pmid: 33638605

journal article

Open Access Collection

Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy

Gong, Ke; Xie, Li; Wu, Zhong‐shi; Xie, Xia; Zhang, Xing‐xing; Chen, Jin‐Lan

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1651pmid: 33661577

journal article

Open Access Collection

Treatment efficacy of high‐dose creatine supplementation in a child with creatine transporter (SLC6A8) deficiency

Shi, Kaili; Zhao, Huimin; Xu, Shuming; Han, Hong; Li, Wenjuan

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1640pmid: 33656256

journal article

Open Access Collection

Targeted next‐generation sequencing of deaf patients from Southwestern China

Li, Yunlong; Su, Jie; Zhang, Jingman; Pei, Jiahong; Li, Dongmei; Zhang, Yinhong; Li, Jingyu; Chen, Menglang; Zhu, Baosheng

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1660pmid: 33724713

journal article

Open Access Collection

Issue Information

2021 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1326pmid: N/A

Showing 1 to 10 of 24 Articles

Previous 1 2 3 Next

Articles per page

Browse All Journals

Related Journals:

Nature Genetics Nucleic Acids Research Genetics Annual Review of Genetics Genomics Mammalian Genome Chromosome Research Journal of Genetics Russian Journal of Genetics