22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 (FOXN1) cause a Thymic Hypoplasia through distinct Developmental Processes
Publication
, Conference
van Oers, NS; Du, Q; Larry, H; Coskun, F; Dozmorov, I; Raj, P; Khan, S; Wysocki, C; Markert, ML; de la Morena, MT
Published in: JOURNAL OF IMMUNOLOGY
May 1, 2019
Duke Scholars
Published In
JOURNAL OF IMMUNOLOGY
EISSN
1550-6606
ISSN
0022-1767
Publication Date
May 1, 2019
Volume
202
Issue
1
Location
San Diego, CA
Publisher
AMER ASSOC IMMUNOLOGISTS
Conference Name
103rd Annual Meeting of the American-Association-of-Immunologists
Related Subject Headings
- Immunology
- 3204 Immunology
- 3101 Biochemistry and cell biology
- 1107 Immunology
Citation
APA
Chicago
ICMJE
MLA
NLM
van Oers, N. S., Du, Q., Larry, H., Coskun, F., Dozmorov, I., Raj, P., … de la Morena, M. T. (2019). 22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 (FOXN1) cause a Thymic Hypoplasia through distinct Developmental Processes. In JOURNAL OF IMMUNOLOGY (Vol. 202). San Diego, CA: AMER ASSOC IMMUNOLOGISTS.
Oers, Nicolai S. van, Qiumei Du, Huynh Larry, Fatma Coskun, Igor Dozmorov, Prithvi Raj, Shaheen Khan, Christian Wysocki, Mary Louise Markert, and Maria Teresa de la Morena. “22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 (FOXN1) cause a Thymic Hypoplasia through distinct Developmental Processes.” In JOURNAL OF IMMUNOLOGY, Vol. 202. AMER ASSOC IMMUNOLOGISTS, 2019.
van Oers NS, Du Q, Larry H, Coskun F, Dozmorov I, Raj P, et al. 22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 (FOXN1) cause a Thymic Hypoplasia through distinct Developmental Processes. In: JOURNAL OF IMMUNOLOGY. AMER ASSOC IMMUNOLOGISTS; 2019.
van Oers, Nicolai S., et al. “22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 (FOXN1) cause a Thymic Hypoplasia through distinct Developmental Processes.” JOURNAL OF IMMUNOLOGY, vol. 202, no. 1, AMER ASSOC IMMUNOLOGISTS, 2019.
van Oers NS, Du Q, Larry H, Coskun F, Dozmorov I, Raj P, Khan S, Wysocki C, Markert ML, de la Morena MT. 22q11.2 Deletion Syndrome (DiGeorge) and Mutations in Forkhead Box N1 (FOXN1) cause a Thymic Hypoplasia through distinct Developmental Processes. JOURNAL OF IMMUNOLOGY. AMER ASSOC IMMUNOLOGISTS; 2019.
Published In
JOURNAL OF IMMUNOLOGY
EISSN
1550-6606
ISSN
0022-1767
Publication Date
May 1, 2019
Volume
202
Issue
1
Location
San Diego, CA
Publisher
AMER ASSOC IMMUNOLOGISTS
Conference Name
103rd Annual Meeting of the American-Association-of-Immunologists
Related Subject Headings
- Immunology
- 3204 Immunology
- 3101 Biochemistry and cell biology
- 1107 Immunology