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Monosomy 7 of Bone Marrow
Known as:
CHROMOSOME 7q DELETION
, Myelodysplasia and Leukemia Syndrome with Monosomy 7
, Bone marrow monosomy 7
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National Institutes of Health
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Related topics
Related topics
6 relations
Broader (5)
Chromosome Deletion
Chromosomes, Human, Pair 7
Congenital chromosomal disease
Leukemia, Myelocytic, Acute
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LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Distal Monosomy 10q Presented as Congenital Hypothyroidism
E. Braha
,
C. Rusu
,
+4 authors
C. Vulpoi
2016
Corpus ID: 78993752
2012
2012
Prenatal Investigation of a Familial Partial Monosomy 10q
Marisa Silva
,
B. Marques
,
+7 authors
H. Correia
2012
Corpus ID: 68068518
2002
2002
21번 염색체 monosomy mosaicism
이영준
,
송지용
,
이상신
,
이석근
,
이혜미
,
차봉근
2002
Corpus ID: 88408255
1998
1998
10q trisomy
N. Mitsufuji
,
Sachiko Tokuda
,
H. Nakanoin
,
H. Yoshioka
,
T. Sawada
1998
Corpus ID: 20912620
Acaseof partial trisomy 10q with partial monosomy 12q is reported. The chromosomal abnormalities resulted from a paternal…
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1985
1985
[Monosomy 9p. Clinical and cytogenetic aspects].
F. Taccone
,
A. M. Fuhrman Conti
,
I. Magnani
,
L. De Luca
La Pediatria Medica e Chirurgica
1985
Corpus ID: 36551002
The Authors describe a new case of monosomy 9 p in a newborn, confirmed by bands technique. The parents had a normal karyotypes…
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1983
1983
Proximal 15q monosomy
Arabella Smith
,
G. Dulk
1983
Corpus ID: 220145530
1983
1983
[Monosomy 18p syndrome with holoprosencephaly].
A. Carratù
,
I. Delaroche
,
P. Tomassini
,
L. Bruni
Minerva Pediatrica
1983
Corpus ID: 27879624
1976
1976
A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-.
J. Davis
,
E. Jenkins
,
H. Klinger
,
R. G. Weed
Cytogenetics and Cell Genetics
1976
Corpus ID: 3282033
Presumptive monosomy for chromosome 21 was found in a male child with multiple malformations and severe psychomotor retardation…
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1976
1976
[Partial deletion of the short arm of the chromosome 9].
F. Serville
,
D. Allain
,
+4 authors
J. Cenraud
Annales de Genetique
1976
Corpus ID: 346357
Monosomy 9p is reported in a boy with trigonocephaly and advanced bone age.
1971
1971
Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
F. Weber
,
R. Sparkes
,
H. Muller
Cytogenetics
1971
Corpus ID: 41548087
Double monosomy mosaicism was observed in a three-year-old girl who had mental and physical retardation. Routine blood-lymphocyte…
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