𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma

✍ Scribed by DR. Nils Mandahl; Helena Willén; Anders Rydholm; Sverre Heim; Felix Mitelman

Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
223 KB
Volume
6
Category
Article
ISSN
1045-2257

No coin nor oath required. For personal study only.

✦ Synopsis

Cytogenetic analysis of a recurrent periosteal chondroma revealed nonreciprocal translocations of both chromosomal segments 12q I 3 +qter, from one chromosome I 2 to 7q32 and from the homologous chromosome I 2 to I6q22. The remaining parts of the two chromosomes I 2 formed a dicentric chromosome. This is the second reported chondroma with a 12q 13-I 5 rearrangement, and changes of t.his chromosome region consequently seem to be nonrandom occurrences in chondromas.

📜 SIMILAR VOLUMES

Involvement of 12q12–13 is a nonrandom c
Involvement of 12q12–13 is a nonrandom chromosome change in renal oncocytoma
✍ Paola Dal Cin; Herman Van den Berghe; Hein Van Poppel; Tania Roskams 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 48 KB

## Involvement of 12q12-13 Is a Nonrandom Chromosome Change in Renal Oncocytoma To the Editors: Cytogenetically, renal oncocytomas constitute a heterogeneous group of benign renal tumors with at least two different subgroups: 1) those with coincident loss of the Y chromosome and chromosome 1, and

Characterization of a complex chromosoma
Characterization of a complex chromosomal rearrangement maps the locus for In vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q 13
✍ Wendy L. Flejter; Lisa D. McDaniel; Minoo Askari; Errol C. Friedberg; Dr. Roger 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 785 KB

## Abstract Microcell‐mediated chromosome transfer (MMCT) is a powerful genetic technique that permits the transfer of a single chromosome from one mammalian cell to another. The utility of MMCT for gene mapping strategies is critically dependent on the careful characterization of the chromosomes b

Maternal origin of a unique extra chromo
Maternal origin of a unique extra chromosome, der(9)(pter?q13::q13?q12:) in a girl with typical trisomy 9p syndrome
✍ Teraoka, Michio ;Narahara, Koji ;Yokoyama, Yuji ;Ninomiya, Shinsuke ;Mizuta, Sho 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 138 KB 👁 1 views

We report on a girl with the typical trisomy 9p syndrome who had an additional E-sized metacentric chromosome. On the basis of GTG-and CBG-banding, her karyotype was considered to be 47,XX,þder(9)(pter!q13:: q13!q12:) de novo. Results of a ¯uorescence in situ hybridization study using a chromosome 9

Follow-up of a report of a potential lin
Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2
✍ Pulver, Ann E. ;Karayiorgou, Maria ;Lasseter, Virginia K. ;Wolyniec, Paula ;Kasc 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 842 KB

from genotyping of 3 dinucleotide repeat polymorphisms (at the loci D22S268, ILSRB, D22S307) for a combined replication sample of 256 families, each having 2 or more affected individuals with DNA, were analysed using a complex autosomal dominant model. This study provided no evidence for linkage or

Deletion mapping of endocrine tumors loc
Deletion mapping of endocrine tumors localizes a second tumor suppressor gene on chromosome band 11q13
✍ Rita Chakrabarti; Eri S. Srivatsan; Thomas F. Wood; Patricia J. Eubanks; Sam A. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 133 KB

Multiple endocrine neoplasia type 1 syndrome (MEN1, MIM 131100), an autosomal dominant disease, is characterized by parathyroid hyperplasia, pancreatic endocrine tumors, and pituitary adenomas. These tumors also occur sporadically. Both the familial (MEN1) and the sporadic tumors reveal loss of hete