𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Recurrence risk in de novo structural chromosomal rearrangements

✍ Scribed by Benno Röthlisberger; Dieter Kotzot

Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
96 KB
Volume
143A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Recurrence Risk in De Novo 21q21q Transl
Recurrence Risk in De Novo 21q21q Translocation Down Syndrome
✍ Hall, Bryan D. ;Opitz, John M. ;Reynolds, James F. 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 113 KB 👁 1 views

## An article by Steinberg et a1 [1984] cautioned against the potential error of counseling families a low-recurrence risk when a previous child has had a de novo 21q21q translocation Down syndrome. They also studied 112 families (ie, sets of parents) with a child with de novo 21q21q translocatio

Prenatal diagnosis of a fetus with two b
Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements
✍ Cotter, Philip D.; Caggana, Michele; Willner, Judith P.; Babu, Arvind; Desnick, 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 321 KB 👁 2 views

T w o apparently balanced chromosome rearrangements were identified in a 17-week fetus by analysis of cultured amniocytes. The fetal karyotype was 46,XX,t(2;16) (q33; q24), inv(7)(p15q11.23). Parental karyotypes were normal, indicating a de novo origin of both chromosome rearrangements in the fetus.

De novo erythroleukemia chromosome featu
De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19
✍ Juan C. Cigudosa; Maria D. Odero; M. José Calasanz; Francesc Solé; Marta Salido; 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 144 KB

## Abstract Erythroid leukemia (ERL or AML‐M6) is an uncommon subtype of acute myeloid leukemia, the clinical, morphological, and genetic behavior of which needs further characterization. We analyzed a homogeneous group of 23 de novo AML‐M6 patients whose bone marrow cells showed complex karyotypes

Prenatal finding of a fetus with mosaici
Prenatal finding of a fetus with mosaicism for two balanced de novo chromosome rearrangements
✍ R. J. Hastings; S. G. Watson; L. S. Chitty 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 117 KB 👁 2 views

Karyotyping of a fetus with mild cerebral ventriculomegaly detected with ultrasound at 23 weeks revealed two apparently balanced structural rearrangements in mosaic form. Using conventional cytogenetics and FISH, the chromosomal constitution was identified as 46,XX,t(3;10)(p13;q21.1),inv(6)(p23q12)/