Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,786,783 papers from all fields of science
Search
Sign In
Create Free Account
22q11.1-q11.2
A chromosome band present on 22q
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
4 relations
22q
Chromosomes
IGL gene
REV1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
[Cytogenetic and molecular genetic analysis of the amniotic fluid cells of a fetus with pseudodicentric isochromosome 22 resulting in partial tetraploidy of 22q].
Yan-yan Shen
,
Hui Kong
,
+6 authors
F. Ding
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2018
Corpus ID: 4849143
OBJECTIVE To diagnose chromosomal abnormalities in amniotic fluid cells by combining karyotyping and single nucleotide…
Expand
2010
2010
Cromosoma 22 en anillo: reporte de un caso en el Hospital de San José
L. Torres
,
Alfonso Suárez
,
Luz Dary Gutiérrez
,
C. Rubio
,
Meilyn Muskus
2010
Corpus ID: 73408059
Paciente de 4 anos, remitido de consulta pediatrica por presentar retraso del desarrollo del lenguaje y dificultad para…
Expand
1999
1999
The human immunoglobulin variable lambda locus IGLV9 gene is a monomorphic marker in the urban Brazilian population.
M. D. da Silva
,
G. Passos
Immunology Letters
1999
Corpus ID: 3199746
Highly Cited
1998
Highly Cited
1998
The Human Immunoglobulin Lambda Variable (IGLV) Genes and Joining (IGLJ) Segments
N. Pallares
,
J. Frippiat
,
V. Giudicelli
,
M. Lefranc
Experimental and Clinical Immunogenetics
1998
Corpus ID: 46770333
The first report of the ‘IMGT Locus on Focus’ section comprises five tables entitled: (1) ‘Number of human germline IGLV genes at…
Expand
1997
1997
EcoRI restriction fragment-length polymorphism of the human immunoglobulin variable lambda 8 (IGLV8) subgroup reveals a gene family.
G. A. Passos Júnior
,
R. G. Queiroz
,
A. Brulé
Human Immunology
1997
Corpus ID: 35784838
Highly Cited
1997
Highly Cited
1997
Another critical region for deletion of 22q11: a study of 100 patients.
Hiroki Kurahashi
,
Etsuko Tsuda
,
+7 authors
I. Nishisho
American journal of medical genetics
1997
Corpus ID: 7732035
Deletions at 22q11.1-q11.2 present with variable manifestations usually referred to as DiGeorge or velo-cardio-facial syndrome…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE