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22q
Known as:
Chromosome 22 Distal Arm
, Chromosome 22 Long Arm
Distal (long) arm of chromosome 22
National Institutes of Health
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Related topics
Related topics
21 relations
22q11
22q11-q13
22q11.1-q11.2
22q11.2
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Colonic Adenocarcinoma in a Patient with Velo Cardio Facial Syndrome (VCFS) and 22q11.2 Microdeletion
Raman Babayeuski
,
V. Ortega
,
C. Mendiola
,
I. Jatoi
,
G. Velagaleti
2016
Corpus ID: 79232704
Colonic Adenocarcinoma in a Patient with Velo Cardio Facial Syndrome (VCFS) and 22q11.2 Microdeletion Colorectal cancer (CRC) is…
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Review
2007
Review
2007
Cat eye syndrome associated with schizophrenia.
M. Domula
,
D. Schulze
,
W. Felber
,
J. Gallinat
,
U. Lang
Pharmacopsychiatry
2007
Corpus ID: 29193821
Schizophrenia is a frequent and complex psychiatric disorder. Current neurobiological research in schizophrenia provides a wealth…
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2005
2005
Stephanie's Story: Caring for a Child With Terminal 22q Deletion Syndrome
S. M. Axel
,
Kathleen Gorman Wermuth
Pediatrics
2005
Corpus ID: 44949458
To the Editor .— I was pleased to read the article “Terminal 22q Deletion Syndrome: A Newly Recognized Cause of Speech and…
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2004
2004
The paternal chromosome 9 and the maternal chromosome 22 are preferentially rearranged in chronic myeloid leukaemia
R. Olício
,
M. B. Rivero
,
H. Seuánez
Leukemia
2004
Corpus ID: 39684387
The paternal chromosome 9 and the maternal chromosome 22 are preferentially rearranged in chronic myeloid leukaemia
2003
2003
p15 INK4b , p14 ARF , and p16 INK4a Inactivation in Sporadic and Neurofibromatosis Type 1-related Malignant Peripheral Nerve Sheath Tumors 1
F. Perrone
,
S. Tabano
,
+6 authors
S. Pilotti
2003
Corpus ID: 30986155
Purpose : Malignant peripheral nerve sheath tumor (MPNST) can arise sporadically or in association with neurofibromatosis type 1…
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2003
2003
Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism?
M. Bonaglia
,
R. Giorda
,
+4 authors
Orsetta Zuffardi
Journal of Medical Genetics
2003
Corpus ID: 31020689
Several papers have recently shown that 6–7% of retarded patients with unclassified malformation syndromes and normal routine…
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2000
2000
Delección en el cromosoma 22 (22q.11.2). Etiología de cardiopatías congénitas troncoconales
Alfonso Buendía Hernández
,
J. C. Colmenero
,
+6 authors
F. Attié
2000
Corpus ID: 162504262
Important advances in the diagnosis and treatment of congenital heart disease (CHD) have been made in the past 50 years. Nowadays…
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1998
1998
Relation of genotype 22 q 11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia – ventricular septal defect
M. Chessa
,
G. Butera
,
+7 authors
D. Bonnet
1998
Corpus ID: 24362523
Objective—To compare the morphology of the pulmonary vessels in tetralogy of Fallot or pulmonary atresia–ventricular septal…
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1992
1992
[Translocation 11q;22q: a clinico-cytogenetic study].
I. V. Lur'e
,
N. V. Rumiantseva
,
+6 authors
M. I. Kuznetsov
Genetika
1992
Corpus ID: 34656693
Seven families with translocations t(11; 22) identified at our Institute and analysis of the literature showed that the imbalance…
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1979
1979
Partial trisomy 22q with elevated arylsulfatase-A activity.
J. Fryns
,
J. Jaeken
,
H. van den Berghe
Annales de Genetique
1979
Corpus ID: 20111295
A two years-old, severely mentally retarded male is reported with 22q trisomy. After the recent confirmation of the localisation…
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