✦ LIBER ✦

A case of retinoblastoma, associated with histiocytosis-X and mosaicism of a deleted D-group chromosome (13q14→q31)

✍ Scribed by E. Orye; Y. Benoit; R. Coppieters; Ph. Jeannin; C. Vercruysse; J. Delaey; M.-J. Delbeke

Book ID: 119839327
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 198 KB
Volume: 22
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.1982.tb01408.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A chromosomal breakpoint that separates

A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31)

✍ John K. Cowell; John Hungerford; Paul Rutland; Marcelle Jay 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 261 KB

A decreasing tendency for cytogenetic ab

A decreasing tendency for cytogenetic abnormality in peripheral lymphocytes of retinoblastoma patients with 13q14 deletion mosaicism

✍ T. Motegi; K. Minoda 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 559 KB

Incidence and Significance of a Deletion

Incidence and Significance of a Deletion of Chromosome Band 13q14 in Patients with Retinoblastoma and in Their Families

✍ Liberfarb, Ruth M.; Bustos, Tania; Miller, Wayne A.; Sang, Delia 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 592 KB

Deficiency of coagulation factors VII an

Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)

✍ R. A. Pfeiffer; R. Ott; S. Gilgenkrantz; P. Alexandre 📂 Article 📅 1982 🏛 Springer 🌐 English ⚖ 507 KB

A case report of a patient with retinobl

A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13

✍ I. Kondo; K. Shin; S. Honmura; H. Nakajima; E. Yamamura; H. Satoh; M. Terauchi; 📂 Article 📅 1985 🏛 Springer 🌐 English ⚖ 436 KB

Retinoblastoma (Rb) occurs in hereditary, non-hereditary, and chromosomal deletion forms and the locus for the Rb gene (Rb-1) is closely linked to the locus for esterase D (ESD) assigned to the chromosome 13q14.11. We describe a patient who was predicted to have Rb from the genetic analysis of the c

A case of del(13)(q14.2)(q31.3) associat

A case of del(13)(q14.2)(q31.3) associated with hypothyroidism, hypertriglyceridemia, hypercholesterolemia and total ophthalmoplegia

✍ Baris Malbora; Cihan Meral; Nihan Malbora; Deniz Sunnetci; Naci Cine; Hakan Savl 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 596 KB