Authors : Guo E; School of Public Health, Guangxi Medical University, 22 Shuang Yong Road, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China. .; School of International Education, Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China. .

Subjects: Multigene Family*; Adenocarcinoma/Adenocarcinoma/Adenocarcinoma/*enzymology ; Adenocarcinoma/Adenocarcinoma/Adenocarcinoma/*genetics

Source: BMC medical genetics [BMC Med Genet] 2020 Jun 15; Vol. 21 (1), pp. 130. Date of Electronic Publication: 2020 Jun 15.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Academic Journal

A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese family.

Authors : Zhang C; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.; Du C

Subjects: Family* ; Genetic Association Studies*/Genetic Association Studies*/Genetic Association Studies*/methods ; Genetic Predisposition to Disease*

Source: BMC medical genetics [BMC Med Genet] 2020 May 29; Vol. 21 (1), pp. 117. Date of Electronic Publication: 2020 May 29.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Academic Journal

A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.

Authors : Shao J; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study

Subjects: Family* ; Genetic Association Studies*/Genetic Association Studies*/Genetic Association Studies*/methods ; Genetic Predisposition to Disease*

Source: BMC medical genetics [BMC Med Genet] 2020 May 27; Vol. 21 (1), pp. 115. Date of Electronic Publication: 2020 May 27.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Academic Journal

Interpreting the MicroRNA-15/107 family: interaction identification by combining network based and experiment supported approach

Authors : Si Wang; Wenhua Zhu; Jing Xu

Subjects: miR-15/107 family; Target gene; Bioinformatics

Source: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-10 (2019)

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Academic Journal

Modeling gene-environment interactions in longitudinal family studies: a comparison of methods and their application to the association between the IGF pathway and childhood obesity

Authors : Cheng Wang; Marie-Hélène Roy-Gagnon; Jean-François Lefebvre

Subjects: Childhood obesity; Insulin-like growth factors; Twin studies

Source: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-16 (2019)

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A nonsense variant in FBN1 caused autosomal dominant Marfan syndrome in a Chinese family: a case report

Authors : Yuping Niu; Sexin Huang; Zeyu Wang

Subjects: Adult; Male; 0301 basic medicine

Source: BMC Med GenetBMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)

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نتائج البحث

فلترة النتائج

Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes

A progressive and complex clinical course in two family members with ERF-related craniosynostosis: a case report

A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss

No association between the Ser9Gly polymorphism of the dopamine receptor D3 gene and schizophrenia: a meta-analysis of family-based association studies

Clinical significance and biological mechanisms of glutathione S-transferase mu gene family in colon adenocarcinoma.

A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese family.

A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.

Interpreting the MicroRNA-15/107 family: interaction identification by combining network based and experiment supported approach

Modeling gene-environment interactions in longitudinal family studies: a comparison of methods and their application to the association between the IGF pathway and childhood obesity

A nonsense variant in FBN1 caused autosomal dominant Marfan syndrome in a Chinese family: a case report

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