
Heteromorphic variants of chromosome 9 - Molecular Cytogenetics
2013年4月1日 · Chromosome 9 presents the highest degree of morphological variations among the non-acrocentric human chromosomes. Variants include 9qh+, 9cenh+, 9ph+, 9qh-, or inv …
Pericentric inversion (Inv) 9 variant—reproductive risk factor or ...
Pericentric inversion 9 is a common chromosome variant with an incidence of approximately 1.6% in the general population [1]. Despite the relatively high incidence of this finding, there is …
Novel pericentric inversion inv(9)(p23q22.3) in unrelated …
2020年5月13日 · Here we report a novel large pericentric inversion of chromosome 9, inv (9) (p23q22.3) in several apparently unrelated carriers, resulting in fertility problems and abnormal …
Acquired inv(9): what is its significance? - PubMed
2005年7月1日 · Pericentric inversion of the heterochromatic region of chromosome 9 [inv(9)] is a common heteromorphism in the general population. It is presumed familial as there are no …
Impact of pericentric inversion of Chromosome 9 [inv (9
Background: One of the frequent occurrences in chromosome rearrangements is pericentric inversion of the Chromosome 9; inv (9) (p11q12), which is consider to be the variant of normal …
Acquired inv(9): what is its significance? - ScienceDirect
2005年7月1日 · Pericentric inversion of the heterochromatic region of chromosome 9 [inv (9)] is a common heteromorphism in the general population. It is presumed familial as there are no …
Pericentric inversion of chromosome 9 [inv (9) (p12q13)]: Its ...
2006年9月1日 · Results: The pericentric inversion frequency of different chromosomes in our study was 1.24% and frequency of inv (9) (p12q13) was high (64.29%) compared to other …
09p120 - Chromosomal Variation in Man - NCBI Bookshelf
A normal male 46,XX,inv(9)(p12q13); a male with Down syndrome 47,XY,+21,inv(9)(p12q13); a premature infant with multiple congenital malformations 46,XX,inv(9)(p12q21), and a Down …
Pericentric inversion 9--incidence and clinical significance
Pericentric inversion of the chromosome 9, inv (9) (p11q13), is such a common occurrence that some cytogeneticists would consider them as normal variants. The incidence is said to be …
Heteromorphic variants of chromosome 9 - PMC
Chromosome 9 presents the highest degree of morphological variations among the non-acrocentric human chromosomes. Variants include 9qh+, 9cenh+, 9ph+, 9qh-, or inv (9) …