Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1573-2592
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment ; volume:41 ; number:5 ; day:13 ; month:5 ; year:2021 ; pages:881-895 ; date:7.2021
Journal of clinical immunology ; 41, Heft 5 (13.5.2021), 881-895, 7.2021
- Creator
-
Collins, Cathleen
Sharpe, Emily
Silber, Abigail
Kulke, Sarah
Hsieh, Elena W. Y.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s10875-021-01059-7
- URN
-
urn:nbn:de:101:1-2021101301571481270384
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:30 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Collins, Cathleen
- Sharpe, Emily
- Silber, Abigail
- Kulke, Sarah
- Hsieh, Elena W. Y.
- SpringerLink (Online service)
Other Objects (12)
Omphalocele: a review of common genetic etiologies
Common genetic etiologies of sensorineural hearing loss in Koreans
Differential diagnosis of ascites: etiologies, ascitic fluid analysis, diagnostic algorithm
AI-based differential diagnosis of dementia etiologies on multimodal data
Shared and distinct genetic etiologies for different types of clonal hematopoiesis
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches
Selective mutism in children : manifestations, diagnosis, therapy
Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Postcraniotomy Headache: Etiologies and Treatments
Sleep related hyper motor epilepsy (SHE): a unique syndrome with heterogeneous genetic etiologies
Omphalocele: a review of common genetic etiologies
Common genetic etiologies of sensorineural hearing loss in Koreans
Differential diagnosis of ascites: etiologies, ascitic fluid analysis, diagnostic algorithm
AI-based differential diagnosis of dementia etiologies on multimodal data
Shared and distinct genetic etiologies for different types of clonal hematopoiesis
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches
Selective mutism in children : manifestations, diagnosis, therapy
Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Postcraniotomy Headache: Etiologies and Treatments
Sleep related hyper motor epilepsy (SHE): a unique syndrome with heterogeneous genetic etiologies
Omphalocele: a review of common genetic etiologies
Common genetic etiologies of sensorineural hearing loss in Koreans
Differential diagnosis of ascites: etiologies, ascitic fluid analysis, diagnostic algorithm
AI-based differential diagnosis of dementia etiologies on multimodal data
Shared and distinct genetic etiologies for different types of clonal hematopoiesis
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches
Selective mutism in children : manifestations, diagnosis, therapy
Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Postcraniotomy Headache: Etiologies and Treatments