✦ LIBER ✦

A subtle deletion of 12p by routine cytogenetics is found to be a translocation to 21q by fluorescence in situ hybridization: t(12;21)(p13;q22)

✍ Scribed by Leonid V. Filatov; Midori Saito; Frederick G. Behm; Gaston K. Rivera; Susana C. Raimondi

Book ID: 113253748
Publisher: Elsevier Science
Year: 1996
Tongue: English
Weight: 384 KB
Volume: 89
Category: Article
ISSN: 0165-4608
DOI: 10.1016/0165-4608(95)00363-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A case of monosomy 21 found to be an unb

A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridization

✍ L. Flaherty; J. Moloney; N. Watson; L. Robson; L. Bousfield; A. Smith 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 137 KB

Translocation (21;22)(q22;q12) in a Ewin

Translocation (21;22)(q22;q12) in a Ewing sarcoma: New case characterized by cytogenetic analysis and fluorescence in situ hybridization of a fresh tumor

✍ F. Mugneret; B. Favre; I. Sidaner; T. Petrella; M. Flesh 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 155 KB

Intrachromosomal gene mapping in man: As

Intrachromosomal gene mapping in man: Assignment of nucleoside phosphorylase to region 14cen→14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation

✍ Uta Francke; Norma Busby; Douglas Shaw; Suzy Hansen; Michael G. Brown 📂 Article 📅 1976 🏛 Springer 🌐 English ⚖ 988 KB

Reassessment of an apparent t(12;17)(p11

Reassessment of an apparent t(12;17)(p11;p11) as an unbalanced t(17;21)(p11;q11) in a case of B-cell chronic lymphocytic leukemia by fluorescence in situ hybridization

✍ Martial Flactif; Jean Luc Laï; Pierre Fenaux 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 322 KB

PRENATAL AND POSTNATAL INVESTIGATION OF

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER–DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

✍ S. L. VAN ZELDEREN-BHOLA; E. J. BRESLAU-SIDERIUS; G. C. BEVERSTOCK; I. STOLTE-DI 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 415 KB 👁 3 views

We present here a case report of a fetus with a kidney anomaly and dilated occipital horns, detected initially by echoscopy at 29 weeks' amenorrhoea. After 31 weeks of gestation, the proband was born with clinical symptoms of Miller-Dieker syndrome. This was subsequently confirmed by fluorescence in

Sperm segregation patterns by fluorescen

Sperm segregation patterns by fluorescence in situ hybridization studies of a 46,XY,t(2;6) heterozygote giving rise to a rare triploid product of conception with a 69,XXY,t(2;6)(p12;q24)der(6)t(2;6)(p12;q24)pat karyotype

✍ A.S.T. Lim; T.H. Lim; S.K. Kee; R. Chieng; S.K. Tay 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 137 KB 👁 2 views