✦ LIBER ✦

Interstitial deletion of 11q13 sequences in HeLa cells

✍ Scribed by Eri S. Srivatsan; Ulla Bengtsson; Pachiappan Manickam; Payam Benyamini; Settara C. Chandrasekharappa; Chi Sun; Eric J. Stanbridge; J. Leslie Redpath

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 393 KB
Volume: 29
Category: Article
ISSN: 1045-2257
DOI: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1024>3.0.co;2-p

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Interstitial deletion 8q11.2-q13 with co

Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE association

✍ Cammon B. Arrington; Brett C. Cowley; Daniel R. Nightingale; Holly Zhou; Arthur 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB 👁 1 views

## Abstract Specific genetic loci responsible for CHARGE association are currently unknown. Herein, we describe a neonate with clinical manifestations consistent with CHARGE association who has a de novo interstitial deletion involving bands 8q11.2 to 8q13. Genetic mapping and genomic microarray te

Molecular breakpoint mapping of 6q11-q14

Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients

✍ Jia-Chi Wang; Linda Dang; Brenda Lomax; Lesley Turner; Mary Shago; Ahmad S. Teeb 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 312 KB 👁 1 views

Enlarged sylvian fissures in infants wit

Enlarged sylvian fissures in infants with interstitial deletion of chromosome 22q11

✍ Bingham, Peter M.; Zimmerman, Robert A.; McDonald-McGinn, Donna; Driscoll, Debor 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 37 KB 👁 2 views

Two infants with chromosome 22q11 deletion syndrome were noted to have symmetrically enlarged Sylvian fissures on cranial MRI. We compared the size of the Sylvian fissures in neuroimaging studies from 17 other subjects with del 22q11 to agematched disease controls. The mean anterior interopercular d

Delineation of an interstitial 9q22 dele

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

✍ S.E. Boonen; D. Stahl; S. Kreiborg; T. Rosenberg; V. Kalscheuer; L.A. Larsen; N. 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 69 KB 👁 2 views

Rare interstitial deletion (2)(p11.2p13)

Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin

✍ Lacbawan, Felicitas L.; White, Beverly J.; Anguiano, Arturo; Rigdon, David T.; B 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 26 KB 👁 1 views

An unbalanced 46,XY,der(2)del(2)(p11.2p13) inv(2)(p11.2q13) karyotype was found in a phenotypically abnormal child with a de novo interstitial deletion of band 2p12 associated with an inv(2)(p11.2q13) inherited from the father. The inv(2) is generally considered a benign familial variant without sig

Gain of 3q and deletion of 11q22 are fre

Gain of 3q and deletion of 11q22 are frequent aberrations in mantle cell lymphoma

✍ Outi Monni; Riikka Oinonen; Erkki Elonen; Kaarle Franssila; Lasse Teerenhovi; He 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 125 KB 👁 1 views

We used comparative genomic hybridization (CGH) to screen for DNA copy number changes in 34 specimens from 27 cases of mantle cell lymphoma (MCL). The most common gains were detected at 3q (52%), 8q (30%), and 15q (26%), whereas the most frequent losses involved 13q (41%), 1p (33%), 6q (30%), 9p (30