Search Results - "Molecular Cytogenetics"

Chromosomal Abnormalities

DOAB: download the publication
DOAB: description of the publication

Primate Cytogenetics and Comparative Genomics

DOAB: download the publication
DOAB: description of the publication

Primate Cytogenetics and Comparative Genomics

OAPEN Library: download the publication
OAPEN Library: description of the publication

Epilepsy and chromosomal abnormalities by Sorge Giovanni, Sorge Anna

Connect to this object online.

Molecular Dermatopathology in Malignant Melanoma by Marie-Annick Reginster, Claudine Pierard-Franchimont, Gérald E. Piérard, Pascale Quatresooz

Connect to this object online.

Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report by Harsh Sheth, Sunil Trivedi, Thomas Liehr, Ketan Patel, Deepika Jain, Jayesh Sheth, Frenny Sheth

Connect to this object online.

Perlman Syndrome with Deletion of DIS3L2 Gene by Salameh K, Viswanathan B, Nawaz Z, Habboub L, Tomerak A, Pattuvalappil R

Connect to this object online.

High-grade B-cell lymphoma with MYC and BCL2 rearrangements arising in a composite lymphoma by Alison M. Moore, Olga Moshkin, Gordon J. Swain, Susan Crocker, David P. LeBrun

Connect to this object online.

Small round cell lesions of the bone: Diagnostic approach, differential diagnoses and impact on treatment by Bharat Rekhi, Asit Mridha, Jayashree Kattoor

Connect to this object online.

Detection of leukemia gene fusions by targeted RNA-sequencing in routine diagnostics by Marie Engvall, Nicola Cahill, Britt-Inger Jonsson, Martin Höglund, Helene Hallböök, Lucia Cavelier

Connect to this object online.

Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances by Luiza Emy Dorfman, Júlio César L. Leite, Roberto Giugliani, Mariluce Riegel

Connect to this object online.

11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies by Xuejiao Chen, Huihui Xu, Weiwu Shi, Feng Wang, Fenfen Xu, Yang Zhang, Jun Gan, Xiong Tian, Baojun Chen, Meizhen Dai

Connect to this object online.

Mutation Breeding in Coffee with Special Reference to Leaf Rust Protocols /

Table of Contents: “…Venecia through somatic embryogenesis -- Protocol on mutation induction in Coffea arabica using in vivo grafting and cuttings -- Protocol on mutation induction in coffee using in vitro tissue cultures -- Screening for resistance to coffee leaf rust -- Protocol to send samples of coffee leaf rust to CIFC -- Coffee leaf rust (Hemileia vastatrix) inoculation and evaluation under laboratory conditions -- Development of a PCR-Based Molecular Detection -- Technique for the Early Diagnosisof Coffee Leaf -- Rust Caused by Hemileia vastatrix -- Protocols for chromosome preparations: molecular cytogenetics and studying genome organization in coffee. .…”
Link to Metadata

Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances by Luiza Emy Dorfman, Júlio César L. Leite, Roberto Giugliani, Mariluce Riegel

Connect to this object online.

The Continuing Value of Ultrastructural Observation in Central Nervous System Neoplasms in Children by Na Rae Kim, Sung-Hye Park

Connect to this object online.

Chronic Lymphocytic Leukemia with t(14;18)(q32;q21) as a Sole Cytogenetic Abnormality by Ghaleb Elyamany, Kamal Fadalla, Hatem Elghezal, Omar Alsuhaibani, Hani Osman, Abdulaziz Al-Abulaaly

Connect to this object online.

Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study by Shuang Hu, Xiangdong Kong

Connect to this object online.

Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Yu-Ling Kuo, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

Connect to this object online.

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis by Chih-Ping Chen, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Yun-Yi Chen, Wayseen Wang

Connect to this object online.

Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements by Chih-Ping Chen, Ming Chen, Yi-Ning Su, Jian-Pei Huang, Gwo-Chin Ma, Shun-Ping Chang, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang

Connect to this object online.