- Title
- Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations.
- Creators
- Chunyun Fu - Guangxi Maternal and Child Health HospitalShiyu Luo - Guangxi Maternal and Child Health HospitalYue Zhang - Guangxi Maternal and Child Health HospitalXin Fan - Guangxi Maternal and Child Health HospitalAlissa M. D'Gama - Dana-Farber/Boston Children's Cancer and Blood Disorders CenterXiaofei Zhang - Guangxi Maternal and Child Health HospitalHaiyang ZhengJiasun Su - Guangxi Maternal and Child Health HospitalChuan Li - Guangxi Maternal and Child Health HospitalJingsi Luo - Guangxi Maternal and Child Health HospitalPankaj B. Agrawal - Dana-Farber/Boston Children's Cancer and Blood Disorders CenterQifei Li - Dana-Farber/Boston Children's Cancer and Blood Disorders CenterShaoke Chen - Guangxi Maternal and Child Health Hospital
- Publication Details
- Clinica chimica acta; international journal of clinical chemistry, Vol.489, pp.103-108
- Publisher
- Elsevier; Netherlands
- Academic Unit
- Miller School of Medicine; UMMG Dept of Pediatrics - Neonatology; UMMG Department of Pediatrics
- Resource Type
- Journal article
- Record Identifier
- 991031926787502976
Journal article
Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations.
Clinica chimica acta; international journal of clinical chemistry, Vol.489, pp.103-108
2018
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7 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.213 Thyroid Disorders
- 1.213.168 Hypothyroidism
- Web Of Science research areas
- Medical Laboratory Technology
- ESI research areas
- Clinical Medicine
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Source: InCites