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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

Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human

Ye, Yuanyuan; Wei, Xiaoli; Sha, Yanwei; Li, Na; Yan, Xiaohong; Cheng, Ling; Qiao, Duanrui; Zhou, Weidong; Wu, Rongfeng; Liu, Qiaobin; Li, Youzhu

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1284pmid: 32410354

journal article

Open Access Collection

CCN6 mutation detection in Chinese patients with progressive pseudo‐rheumatoid dysplasia and identification of four novel mutations

Wang, Yingjie; Xiao, Ke; Yang, Yuemei; Wu, Zhihong; Jin, Jin; Qiu, Guixing; Weng, Xisheng; Zhao, Xiuli

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1261pmid: 32351055

journal article

Open Access Collection

Children from nuclear families with bad parental relationship could develop tic symptoms

Zhu, Pengcheng; Wu, Min; Huang, Pinxian; Zhao, Xin; Ji, Xiaoyi

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1286pmid: 32419379

journal article

Open Access Collection

Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review

Liu, Yaobin; Mapow, Beth

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1265pmid: 32400031

journal article

Open Access Collection

Missense NR2F1 variant in monozygotic twins affected with the Bosch–Boonstra–Schaaf optic atrophy syndrome

Mio, Catia; Fogolari, Federico; Pezzoli, Laura; D’Elia, Angela V.; Iascone, Maria; Damante, Giuseppe

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1278pmid: 32412696

journal article

Open Access Collection

Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers

Kozina, Anastasiya A.; Okuneva, Elena G.; Baryshnikova, Natalia V.; Kondakova, Olga B.; Nikolaeva, Ekaterina A.; Fedoniuk, Inessa D.; Mikhailova, Svetlana V.; Krasnenko, Anna Y.; Stetsenko, Ivan F.; Plotnikov, Nikolay A.; Klimchuk, Olesia I.; Popov, Yaroslav V.; Surkova, Ekaterina I.; Shatalov, Peter A.; Rakitko, Alexander S.; Ilinsky, Valery V.

2020 Molecular Genetics & Genomic Medicine

journal article

Open Access Collection

Acromicric dysplasia with stiff skin syndrome‐like severe cutaneous presentation in an 8‐year‐old boy with a missense FBN1 mutation: Case report and literature review

Wang, Tao; Yang, Yuyan; Dong, Qi; Zhu, Huijuan; Liu, Yuehua

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1282pmid: 32406602

journal article

Open Access Collection

Sequential multiple retinal vein occlusions and transient ischemic attack in MTHFR polymorphism and protein S deficiency

Cho, Ahra; Ragi, Sara D.; Oh, Jin Kyun; Lima de Carvalho, Jose Ronaldo; Ryu, Joseph; Yang, Ber‐Yuh; Tsang, Stephen H.

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1273pmid: 32347013

journal article

Open Access Collection

The pedigree analysis and prenatal diagnosis of Hong Kongαα Thalassemia and the sequence analysis of Hong Kongαα Allele

Wang, Wenjuan; Zheng, Haiqing; Zeng, Dan; Jiang, Linbin; Yu, Donglan; Yang, Yuzhong; Feng, Qiao; Xia, Yang; Zhu, Chunjiang

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1285pmid: 32419356

journal article

Open Access Collection

Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome

Lombardo, Barbara; D'Argenio, Valeria; Monda, Emanuele; Vitale, Andrea; Caiazza, Martina; Sacchetti, Lucia; Pastore, Lucio; Limongelli, Giuseppe; Frisso, Giulia; Mazzaccara, Cristina

2020 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.1260pmid: 32396277

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

doi: 10.1002/mgg3.1228pmid: 32412666