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CONOTRUNCAL ANOMALY FACE SYNDROME
Known as:
CAFS
, Conotruncal Anomaly Face Syndrome (CTAF)
National Institutes of Health
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Related topics
Related topics
1 relation
DiGeorge Syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
CD61+ and CAF+ were found to be good prognosis factors for invasive breast cancer patients.
Dong-yan Cai
,
Xiao-hong Wu
,
Tingting Hong
,
Y. Mao
,
Xiaosong Ge
,
D. Hua
Pathology, Research and Practice
2017
Corpus ID: 41878763
2010
2010
Chemical aerosol flow synthesis of hollow metallic aluminum particles
Richard J. Helmich
,
K. Suslick
2010
Corpus ID: 97709325
A novel aerosol synthesis of hollow 300 nm spheres of Al was achieved using an ultrasonic spray technique without the use of…
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2007
2007
Algorithm for the charge-coupled-device scanning actinic flux spectroradiometer ozone retrieval in support of the Aura satellite validation
I. Petropavlovskikh
,
R. Shetter
,
S. Hall
,
K. Ullmann
,
P. Bhartia
2007
Corpus ID: 56060118
Stratospheric ozone column data was acquired during four recent aircraft-based validation missions for the Aura satellite flown…
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2006
2006
A Novel Feature Selection Method Based on Category Information Analysis for Class Prejudging in Text Classification
Qiang Wang
,
Yi Guan
,
Xiaolong Wang
,
Zhi-ming Xu
2006
Corpus ID: 11579429
Summary This paper presents a new feature selection algorithm with the category information analysis in text classification. The…
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1999
1999
Double-lumen aortic arch with anomalous left pulmonary artery origin from the main pulmonary artery--bilateral persistent fifth aortic arch--a case report.
J. N. Wang
,
J. Wu
,
Y. Yang
International Journal of Cardiology
1999
Corpus ID: 22505292
Review
1997
Review
1997
Chromosome 22q1l Deletion Syndrome: An Update and Review for the Primary Pediatrician
J. Thomas
,
J. Graham
La Clinica pediatrica
1997
Corpus ID: 34200721
Chromosome 22ql1 deletion syndrome is a relatively newly described syndrome that encompasses the majority of patients previously…
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1996
1996
Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
D. McDonald-McGinn
,
B. Emanuel
,
E. Zackai
American journal of medical genetics
1996
Corpus ID: 43160898
1996
1996
Size of 22q deletions in four previously reported patients with conotruncal anomaly face syndrome
J. Pierpont
,
R. Erickson
,
F. Thompson
,
Jin-Ming Yang
Clinical Genetics
1996
Corpus ID: 30635388
Conotruncal anomaly face syndrome (CTAFS) was distinguished from velo‐cardio‐facial syndrome (VCFS) in a bind study, yet shared…
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1996
1996
Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region.
Elizabeth Goldmuntz
,
Zhili Wang
,
Bruce A. Roe
,
M. Budarf
Genomics
1996
Corpus ID: 33655540
DiGeorge syndrome (DGS) and velocardiofacial syndrome have been shown to be associated with microdeletions of chromosomal regions…
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1963
1963
The Fluorescent Antibody Technique Applied to Titration and Identification of Antigens in Solutions or Antisera.∗
F. Paronetto
Proceedings of the Society for Experimental…
1963
Corpus ID: 30726067
Summary Cellulose acetate discs or agar are useful supporting media for titration or identification of antigen or antibody. The…
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