Suchergebnisse - "Guo, Tingwei"

PubPharm (47)

1

A novel small deletion of LMX1B in a large Chinese family with nail-patella syndrome

enthalten in: BMC medical genetics | 2019

von Yan, X. | Lin, J. | Wang, Y. | +4

2

A novel small deletion of LMX1B in a large Chinese family with nail-patella syndrome

enthalten in: BMC medical genetics | 2019

von Yan, X. | Lin, J. | Wang, Y. | +4

3

A novel small deletion of LMX1B in a large Chinese family with nail-patella syndrome

enthalten in: BMC medical genetics | 2019

von Yan, X. | Lin, J. | Wang, Y. | +4

4

Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

enthalten in: American journal of medical genetics. Part A | 2018

von Zhao, Y. | Guo, T. | Fiksinski, A. | +42

5

Retraction Notice to : Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements

enthalten in: American journal of human genetics | 2018

von Demaerel, W. | Hestand, M. | Vergaelen, E. | +89

RetractionOf: Am J Hum Genet. 2017 Oct 5;101(4):616-622. - PMID 28965848

6

HLA-B*07, HLA-DRB1*07, HLA-DRB1*12, and HLA-C*03:02 Strongly Associate With BMI : Data From 1.3 Million Healthy Chinese Adults

enthalten in: Diabetes | 2018

von Shen, J. | Guo, T. | Wang, T. | +48

7

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2

enthalten in: Human molecular genetics | 2018

von Guo, T. | Diacou, A. | Nomaru, H. | +28

8

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

enthalten in: The American journal of psychiatry | 2017

von Bassett, A. | Lowther, C. | Merico, D. | +48

CommentIn: Am J Psychiatry. 2017 Nov 1;174(11):1027-1029. - PMID 29088933

9

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

enthalten in: Circulation. Cardiovascular genetics | 2017

von Guo, T. | Repetto, G. | McDonald McGinn, D. | +44

CommentIn: Circ Cardiovasc Genet. 2017 Oct;10(5):. - PMID 29025762

10

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements

enthalten in: American journal of human genetics | 2017

von Demaerel, W. | Hestand, M. | Vergaelen, E. | +89

RetractionIn: Am J Hum Genet. 2018 Sep 6;103(3):457. - PMID 30193139

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