Green Journals

Retraction Note: lncRNA TINCR sponges miR-214-5p to upregulate ROCK1 in hepatocellular carcinoma

Min Hu, Yaowu Han, Ying Zhang et al.

2020-12 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01178-9

A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population

Jung Yeon Seo, Joong-Gon Shin, Byeong Ju Youn et al.

2020-12 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01177-w

DGAT1 mutations leading to delayed chronic diarrhoea: a case report

Luojia Xu, Weizhong Gu, Youyou Luo et al.

2020-12 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01164-1

Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis

Mouna Ouhenach, Abdelali Zrhidri, Imane Cherkaoui Jaouad et al.

2020-12 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01167-y

Case report: progressive familial intrahepatic cholestasis type 3 with compound heterozygous ABCB4 variants diagnosed 15 years after liver transplantation

Mariam Goubran, Ayodeji Aderibigbe, Emmanuel Jacquemin et al.

2020-11-30 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01173-0

First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report

Nicole Weisschuh, Pascale Mazzola, Tilman Heinrich et al.

2020-11-26 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01166-z

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient

Ciliu Zhang, Xiaolu Deng, Yafei Wen et al.

2020-11-26 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01162-3

Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype

Rüdiger Schultz, Varpu Elenius, Heikki Lukkarinen et al.

2020-11-26 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01171-2

Next generation sequencing of RB1gene for the molecular diagnosis of ethnic minority with retinoblastoma in Yunnan

Zhen Zhang, Yi-shuang Xiao, Ru Shen et al.

2020-11-23 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01150-7

Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection

Sally N. Adebamowo, Adebowale A. Adeyemo, Charles N. Rotimi et al.

2020-11-23 Vol. 21 Issue 1

DOI: 10.1186/s12881-020-01156-1

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Recent Articles

Retraction Note: lncRNA TINCR sponges miR-214-5p to upregulate ROCK1 in hepatocellular carcinoma

A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population

DGAT1 mutations leading to delayed chronic diarrhoea: a case report

Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis

Case report: progressive familial intrahepatic cholestasis type 3 with compound heterozygous ABCB4 variants diagnosed 15 years after liver transplantation

First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient

Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype

Next generation sequencing of RB1gene for the molecular diagnosis of ethnic minority with retinoblastoma in Yunnan

Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection