bac/pac array slide (Integragen sa)
90
Structured Review
Integragen sa
bac/pac array slide
Bac/Pac Array Slide, supplied by Integragen sa, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bac+array+slide/bac+pac+array+slide/pm17702013-39-22-25
Average 90 stars, based on 1 article reviews
Bac/Pac Array Slide, supplied by Integragen sa, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bac+array+slide/bac+pac+array+slide/pm17702013-39-22-25
Average 90 stars, based on 1 article reviews
bac/pac array slide - by Bioz Stars,
2026-11
90/100 stars
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other:Article Title: Pure segmental trisomy 1q42-qter in a boy with a severe phenotype. Article Snippet: Since the early 1970s [Van den Berghe et al., 1973], several communications have described a distinct phenotype for the partial trisomy of the long arm of chromosome 1 and, after more than 100 cases reported so far, three hotspot breakpoints have been localized in the 1 long arm: q25 (only interstitial duplications have been described) [Schinzel, 1979], q32 [Duba et al., 1997], and q42 [Chia et al., 1988].. After delineating the common clinical features of a trisomy 1q phenotype, a tentative genotype/phenotype correlation has been made by grouping the signs according to the length of the duplicated segment: mental retardation, cranial abnormalities, hypertelorism, highly arched palate, malformation of the ears and of the toes have been foundpresent in all the cases, regardless of the length of the trisomic segment.. Due to this fact, those manifestations have been assigned to the baseline phenotype of trisomy 1q syndrome, and have been attributed to the common and moredistal region, i.e., the 1q42->qter [Barros-Nunez et al., 1989]; moreover, various malformations (ocular, cardiac, urinary, gastrointestinal) have been observed to be superimposed on the common phenotype with an increased frequency in those cases with a larger trisomic imbalance [Gfatter et al., 1998]. |