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X chromosome, monosomy Xp22 pter
Known as:
Deletion Xp22 pter
, Monosomy Xp22 pter
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
Chromosome Deletion
Sex Chromosome Aberrations
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
CML with complex chromosome rearrangements and dysplastic megakaryocytes.
Zhaodong Xu
,
J. McGowan-Jordan
Blood
2016
Corpus ID: 206944192
![Figure][1] A 41-year-old man presented with anemia (hemoglobin 112 g/dL), leukocytosis (white blood cells 158.85 × 109/L…
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2010
2010
피부 질환, 손상 또는 상처의 예방 및/또는 치료에 유용한 프테로스틸벤
호세 마리아 에스트렐라 아리쿠엘
,
미구엘 에이. 아쎈씨 미랄레스
2010
Corpus ID: 189043946
본 발명은 피부 질환, 손상 또는 상처를 예방 및/또는 치료하기 위한 약제학적 조성물의 제조에 사용되는 PTER, 또는 이의 임의의 허용성 염, 경우에 따라 QUER 또는 이의 임의의 허용성 염과 배합된 PTER…
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2007
2007
IMAGE ORIENTATION BY GPS AND INS
H. Burman
2007
Corpus ID: 15268421
This paper deals with GPS and INS for georeferencin g data collected by airborne imaging sensors. It go es through the basic…
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Highly Cited
2006
Highly Cited
2006
Characterisation of dic(9;20)(p11–13;q11) in childhood B‐cell precursor acute lymphoblastic leukaemia by tiling resolution array‐based comparative genomic hybridisation reveals clustered breakpoints…
J. Schoumans
,
B. Johansson
,
+9 authors
A. Nordgren
British Journal of Haematology
2006
Corpus ID: 22597198
Although the dic(9;20)(p11–13;q11) is a recurrent chromosomal abnormality in paediatric B‐cell precursor acute lymphoblastic…
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2006
2006
Pter Halsz 19432006
Judith "Galus" Halasz
The Drama Review
2006
Corpus ID: 57564502
1995
1995
Assignment of the rat Variable Coding Sequence (VCS) gene family to Chromosome 14
I. Rosinski-Chupin
,
T. Kuramoto
,
Y. Courty
,
F. Rougeon
,
T. Serikawa
Mammalian Genome
1995
Corpus ID: 1551709
genes in this species by use of cell hybrids. We had overcome the problem of MAU segregation by MMCT and reported the assignment…
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1995
1995
Precise ordering of 26 cosmid markers on chromosome region 3p23-->p21.3 by two-color FISH on human prophase chromosomes and stretched DNAs.
T. Ariyama
,
T. Kimura
,
K. Yamakawa
,
Y. Nakamura
,
T. Abe
,
J. Inazawa
Cytogenetics and Cell Genetics
1995
Corpus ID: 46861133
To construct a detailed cytogenetic map of human chromosome region 3p23-->p21.3, we determined the order of 26 cosmid markers…
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1993
1993
Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.
M. A. Pericak-Vance
,
K J Nunes
,
+7 authors
H. A. Drabkin
Journal of Medical Genetics
1993
Corpus ID: 10308160
A genetic map of highly polymorphic microsatellite markers spanning the von Hippel-Lindau region (VHL) of 3p25 was constructed…
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Review
1992
Review
1992
Population cytogenetics of aphidicolin-induced fragile sites
B. Tedeschi
,
P. Vernole
,
M. Sanna
,
B. Nicoletti
Human Genetics
1992
Corpus ID: 2937617
SummaryChromosome fragile sites are inducible by aphidicolin in cultured human lymphocytes. To assess the frequency and…
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1986
1986
Morphology alone does not make an isochromosome
S. Schmutz
,
E. Pinno
Human Genetics
1986
Corpus ID: 42159413
SummaryIsochromosomes are chromosomes with genetically identical arms. Chromosomes morphologically similar to isochromosomes can…
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