Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9

1996 ◽  
Vol 98 (5) ◽  
pp. 576-580 ◽  
Author(s):  
R. V. Samonte ◽  
Robert A. Conte ◽  
K. H. Ramesh ◽  
R. S. Verma
Keyword(s):  
Human Chromosome ◽  
Chromosome 9 ◽  
Molecular Cytogenetic ◽  
Pericentric Inversions ◽  
Cytogenetic Characterization

Preparation and molecular cytogenetic characterization of ?-satellite DNA of human chromosome 6

1989 ◽  
Vol 107 (6) ◽  
pp. 861-864
Author(s):  
I. V. Gar'kavtsev ◽  
T. G. Tsvetkova ◽  
E. V. Maksimova ◽  
M. E. Gonzales-Patino
Keyword(s):  
Human Chromosome ◽  
Satellite Dna ◽  
Chromosome 6 ◽  
Molecular Cytogenetic ◽  
Cytogenetic Characterization ◽  
Human Chromosome 6

Clinical and molecular cytogenetic characterization of two cases of inverted duplication deletion 8p

2020 ◽  
pp. 41-42
Author(s):  
Д.А. Юрченко ◽  
М.Е. Миньженкова ◽  
Е.Л. Дадали ◽  
Н.В. Шилова
Keyword(s):  
Mental Retardation ◽  
Congenital Heart ◽  
Heart Defects ◽  
Clinical Manifestations ◽  
Formation Mechanisms ◽  
Agenesis Of Corpus Callosum ◽  
Molecular Cytogenetic ◽  
Inverted Duplication ◽  
Cytogenetic Characterization

Синдром инвертированной дупликации короткого плеча хромосомы 8 со смежной терминальной делециенй (inv dup del(8p), ORPHA 96092) - редкая хромосомная аномалия (ХА) с частотой 1/10000-1/30000 живорожденных. В статье представлены клинические и молекулярно-цитогенетические характеристики двух неродственных пациентов с синдромом inv dup del(8p) и уточнены механизмы формирования хромосомного дисбаланса. Inverted duplication deletion 8p syndrome (inv dup del(8p), ORPHA 96092) is a rare chromosomal abnormality with a frequency of 1:10,000 - 30,000 newborns. Clinical manifestations of this syndrome include mental retardation, facial anomalies, hypoplasia/agenesis of corpus callosum, scoliosis and/or kyphosis, hypotonia, congenital heart defects. The article presents the clinical and molecular cytogenetic characteristics of two patients with inv dup del (8p) syndrome and clarifies the formation mechanisms.

scholarly journals Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1

2018 ◽  
Vol Volume 11 ◽  
pp. 77-80 ◽  
Author(s):  
Isabel Ochando ◽  
Melanie Cristine Alonzo Martínez ◽  
Ana María Serrano ◽  
Antonio Urbano ◽  
Eduardo Cazorla ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
De Novo ◽  
Molecular Cytogenetic ◽  
Cytogenetic Characterization

Molecular cytogenetic characterization of 1p deletions and 1;17 translocation breakpoints in neuroblastoma

1994 ◽  
Vol 77 (2) ◽  
pp. 157
Author(s):  
Nadine Van Roy ◽  
Geneviève Laureys ◽  
Ngan Ching Cheng ◽  
Ghislain Opdenakker ◽  
Rogier Versteeg ◽  
...  
Keyword(s):  
Molecular Cytogenetic ◽  
Translocation Breakpoints ◽  
Cytogenetic Characterization
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