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17q
Known as:
Chromosome 17 Distal Arm
, Chromosome 17 Long Arm
Distal (long) arm of chromosome 17
National Institutes of Health
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Related topics
Related topics
40 relations
17q11
17q11-q12
17q11-q21
17q11-qter
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Pericytic (Perivascular) Tumors.
Henryk A Domansk
,
Charles S Walther
Monographs in clinical cytology
2017
Corpus ID: 207595875
2008
2008
Copy number variation at the breakpoint region of isochromosome 17 q
C. Carvalho
,
J. Lupski
2008
Corpus ID: 40857934
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
Molecular and Functional Analysis of PRKAR 1 A and its Locus ( 17 q 22 – 24 ) in Sporadic Adrenocortical Tumors : 17 q Losses , Somatic Mutations , and Protein Kinase A Expression and Activity 1
J. Bertherat
,
L. Groussin
,
+11 authors
C. Stratakis
2003
Corpus ID: 42876410
Germ-line protein kinase A (PKA) regulatory-subunit type-I (RI ; PRKAR1A)-inactivating mutations and loss-of-heterozygosity (LOH…
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2002
2002
Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q
M. Hitchins
,
S. Abu-Amero
,
+4 authors
G. Moore
Journal of Medical Genetics
2002
Corpus ID: 33911476
Silver-Russell syndrome (SRS) (MIM 180860) is characterised by intrauterine and postnatal growth restriction, in association with…
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1999
1999
Isochromosome 17 q in Blast Crisis of Chronic Myeloid Leukemia and in Other Hematologic Malignancies Is the Result of Clustered Breakpoints in 17 p 11 and Is Not Associated With Coding TP 53…
T. Fioretos
,
B. Strömbeck
,
+8 authors
M. Höglund
1999
Corpus ID: 26231845
An isochromosome of the long arm of chromosome 17, i(17q), is the most frequent genetic abnormality observed during the disease…
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1993
1993
Probable denovo 17qduplication (qi1 .2-+q21.1): a newlyrecognised chromosomal syndrome ina child withKlinefelter's syndrome
A. Butt
,
D. Mehta
,
F. Flinter
1993
Corpus ID: 26732060
A childisdescribed witha previously unreported probabletrisomyfora segmentofthelongarm ofchromosome17 responsible forsome…
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1990
1990
Acute nonlymphocytic leukemia (ANLL) with isochromosome i(17q) as the sole chromosomal anomaly: a distinct entity?
H. Weh
,
Rolf Kuse
,
D. Hossfeld
European Journal of Haematology
1990
Corpus ID: 10076028
Abstract: 3 patients with acute nonlymphocytic leukemia (ANLL) and an isochromosome (17q) as the sole chromosomal defect are…
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1981
1981
Translocation (5p; 17q) in blast crisis of chronic myeloid leukemia.
A. Hagemeijer
,
W. Sizoo
,
E. Smit
,
J. Abels
Cytogenetics and Cell Genetics
1981
Corpus ID: 3323810
A new abnormality of chromosome 17, distinct from i(17q), was observed in bone marrow cells of two patients with CML during a…
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1979
1979
Assignment of the human acid alpha-glucosidase gene (alphaGLU) to chromosome 17 using somatic cell hybrids.
E. Solomon
,
D. Swallow
,
S. Burgess
,
L. Evans
Annals of Human Genetics
1979
Corpus ID: 28651210
Hybrid clones (MOGs) were made between the mouse line RAG and a primary fibroblast line from an individual of the rare alphaGLU 2…
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