𝔖 Bobbio Scriptorium
✦   LIBER   ✦

De novo nonreciprocal translocation 1;8 confirmed by fluorescent in situ hybridization

✍ Scribed by Wiley, John E. ;Stout, Janice C. ;Palmer, Shane M. ;Kushnick, Theodore


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
173 KB
Volume
57
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Trisomy 22 confirmed by fluorescent in s
✍ Stratton, Robert F. ;DuPont, Barbara R. ;Mattern, Vicki L. ;Young, Robert S. ;Mc πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 421 KB πŸ‘ 2 views

We report on a newborn girl with multiple congenital anomalies, whose G-banded chromosome analysis showed complete trisomy 22. Chromosome painting using a whole-chromosome painting probe for chromosome 22 confirmed that neither chromosome 22 was involved in a cryptic translocation.

Prenatal detection of de novo duplicatio
✍ Li, Shibo; Tuck-Muller, Cathy M.; MartοΏ½nez, JosοΏ½ E.; Rowley, Ewellonda R.; Chen, πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 14 KB πŸ‘ 2 views

We present a patient with developmental delay, minor anomalies, and duplication 18p confirmed by fluorescence in situ hybridization with whole chromosome 18 painting probe (Oncor p5218). Our observation confirms the findings of other investigators that duplication 18p is not associated with major ma

Simultaneous detection of MYC, BVR1, and
✍ Katrina Rack; Eric Delabesse; Isabelle Radford-Weiss; Priscille Bourquelot; GaΓ«l πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 232 KB πŸ‘ 1 views

The rapid detection of chromosome band 8q24 rearrangements, including classical translocations involving MYC and variant 3Ј translocations, is important for the accurate diagnosis and appropriate treatment of lymphoid malignancies. We have identified and characterized a CEPH YAC, 934e1, which extend

Characterization of a de novo unbalanced
✍ Engelen, John J.M.; Loots, Wil J.G.; Albrechts, Jozefa C.M.; Plomp, Astrid S.; v πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 37 KB πŸ‘ 2 views

We report on a patient with a de novo translocation between the long arms of chromosomes 14 and 18. The translocation was studied using microdissection in combination with fluorescence in situ hybridization (micro-FISH). Five copies of the chromosomes involved in the translocation were isolated by m

FULL MONOSOMY 21, PRENATALLY DIAGNOSED B
✍ ANNE M. S. JOOSTEN; SANDRA DE VOS; DIANE VAN OPSTAL; HELEN BRANDENBURG; JOHANNES πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 442 KB πŸ‘ 1 views

We describe a case of full monosomy 21 which was prenatally diagnosed in chorionic villi by fluorescent in situ hybridization (FISH). Because of intrauterine fetal death, a curettage was performed and cytogenetic analysis of skin fibroblasts confirmed the presence of monosomy 21 in fetal cells. DNA