Results 261 to 270 of about 2,497,717 (340)

An evolutionarily conserved early replicatig segment on the sex chromosomes of man and great apes [PDF]

, 1986
Schempp, Werner, Weber, Bernhard, Wiesner, Henning   +2 more
core  

Chromosome Banding and DNA Methylation Patterns, Chromatin Organisation and Nuclear DNA Content in Zingeria biebersteiniana

Biologia plantarum, 2003
R. Cremonini, M. R. Castiglione, V. G. Grif, V. Kotseruba, E. O. Punina, A. V. Rodionov, O. Muravenko, K. Popov, T. Samatadze, Alexander V. Zelenin   +9 more
semanticscholar   +1 more source

Aortic atresia, interrupted hypoplastic right aortic arch, single ventricle and bilateral arterial duct - a unique anatomy with surgical palliation. [PDF]

J Cardiothorac Surg
Malec E, Dryzek P, Blasiak J, Januszewska K.   +3 more
europepmc   +1 more source

Endonuclease banding reveals that atrazine-induced aneuploidy resembles spontaneous chromosome loss in Crassostrea gigas

, 2005
Karine Bouilly, Alexandra Leitão, Raquel Chaves, Henrique Guedes‐Pinto, Pierre Boudry, Sylvie Lapègue   +5 more
openalex   +2 more sources

Chromosome banding studies in 106 cases of chronic myelogenous leukemia

The Japanese Journal of Human Genetics, 1982
T. Tomiyasu, M. Sasaki, K. Kondo, M. Okada   +3 more
semanticscholar   +1 more source

Breast Findings in Females With Beckwith–Wiedemann Syndrome

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Beckwith–Wiedemann syndrome (BWS) is an overgrowth condition caused by epigenetic defects on chromosome 11p15. Children with BWS have a predisposition to embryonal tumors such as Wilms tumor and hepatoblastoma. However, few reports of breast tumors in females with BWS have been published and the risk of malignancy and need for screening ...
Liron D. Grossmann, Andrew M. George, Tom Lapidus, Cassandra Ligh, Suzanne P. MacFarland, Jennifer M. Kalish   +5 more
wiley   +1 more source

A Long-Term Survival Case of Acute Myeloid Leukemia With MYC-Positive Double Minute Chromosomes. [PDF]

Cureus
Yoshimaru R, Kuzume A, Nakamura H, Guo YM, Chi S, Nakamura S, Iida M, Kawamura K, Akie K, Minami Y, Yuda J.   +10 more
europepmc   +1 more source

Functional analysis of CBFA2T3 : a breast cancer tumour suppressor from chromosome band 16q24.3.

, 2009
Zarqa Saif
openalex   +1 more source

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

Prenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell, Samantha Stover, Nora Gibson, Timothy Olson, James Connelly, Matthew Grace, Jennifer Andrews   +6 more
wiley   +1 more source

Chromosomal Abnormalities in Recurrent Pregnancy Loss at a Tertiary Care Center. [PDF]

Cureus
Sinha MB, Thakur P, Verma R.
europepmc   +1 more source