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Chromosome 6, monosomy 6q
Known as:
Deletion 6q
, Monosomy 6q
National Institutes of Health
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2 relations
Broader (2)
Chromosome Deletion
Chromosomes, Human, Pair 6
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Congenital hydrocephalus and hemivertebrae associated with de novo partial monosomy 6q (6q25.3→qter)
Y. Li
,
K. Choy
,
+8 authors
X.-J. Chen
Balkan Journal of Medical Genetics
2015
Corpus ID: 13599227
Abstract This study was conducted to describe a prenatal case of congenital hydrocephalus and hemivertebrae with a 6q terminal…
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2003
2003
Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations
S. Cavani
,
C. Perfumo
,
+7 authors
M. Pierluigi
Prenatal Diagnosis
2003
Corpus ID: 13482340
Here we describe a foetus with intrauterine growth retardation (IUGR), cerebral malformations and a 46,XY,der(1),t(1;6)(p36.3;q25…
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2003
2003
Severe sensory hearing loss in del(6q)-syndrome.
M. Schuster
,
J. Lohscheller
,
P. Kummer
,
U. Eysholdt
,
F. Rosanowski
International Journal of Pediatric…
2003
Corpus ID: 19875019
1996
1996
PARTIAL TRISOMY/MONOSOMY 6q IN FETAL CELLS AND CVS LONG‐TERM CULTURE NOT PRESENT IN CVS SHORT‐TERM CULTURE
R. Wegner
,
E. Schröck
,
M. Obladen
,
R. Becker
,
M. Stumm
,
K. Sperling
Prenatal Diagnosis
1996
Corpus ID: 35411775
A cytogenetic discrepancy in chorionic villi with implications for prenatal diagnosis is described. Chromosome analysis revealed…
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1993
1993
Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion
Jan Wauters
,
P. Bossuyt
,
L. Roelen
,
B. Roy
,
Jan E. Dumon
Clinical Genetics
1993
Corpus ID: 45382276
Wauters JG, Bossuyt PJ, Roelen L, van Roy B, Dumon J. Application of fluorescence in situ hybridization for early prenatal…
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1987
1987
A child with partial monosomy 6q secondary to a maternal direct insertional event.
S. Matkins
,
J. Meyer
,
A. Berry
Journal of Medical Genetics
1987
Corpus ID: 45799408
We report a child, now aged two years, who is monosomic for the region 6q23.1----q24.2. Her mother, older sister, and twin sister…
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