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MeSH:(Cytogenetic Analysis)

1.Clinical and Laboratory Characteristics of Acute Myeloid Leukemia, Myelodysplasia-Related.

Wei-Bin LI ; Lan YANG ; Shao-Jie CHENG ; Ya CHEN ; Yan JIANG

Journal of Experimental Hematology 2025;33(3):666-671

2.Review of Cytogenetic findings of patients with turner syndrome and its variants in Filipinos and the implications in genetic counseling.

Ebner Bon Gatus MACEDA ; Michelle Espinoza ABADINGO ; Cheryll MAGBANUA-CALALO ; Edsel Allan G. SALONGA ; Jonathan Z. OBLEFIAS ; Maria Melanie Liberty Bandagosa ALCAUSIN

Philippine Journal of Health Research and Development 2025;29(4):72-77

3.ChromTR: chromosome detection in raw metaphase cell images via deformable transformers.

Chao XIA ; Jiyue WANG ; Xin YOU ; Yaling FAN ; Bing CHEN ; Saijuan CHEN ; Jie YANG

Frontiers of Medicine 2024;18(6):1100-1114

4.Fibroma of tendon sheath: a clinicopathological and genetic analysis of 134 cases.

Jian CUI ; Ya LU ; Yan QIU ; Xin HE ; Min CHEN ; Hong Ying ZHANG

Chinese Journal of Pathology 2023;52(4):364-369

5.Clinicopathological features of gastric carcinomas with NTRK-rearrangement/amplification: report of four cases.

An Di XU ; Yao FU ; Xiao Hong PU ; Hong Yan WU ; Qi SUN ; Xiang Shan FAN

Chinese Journal of Pathology 2023;52(5):454-459

6.Clinicopathological features of fibrin-associated diffuse large B-cell lymphoma: a report of six cases.

Lan SUN ; Peng LI ; Xiao Ge ZHOU ; Xiao Jing TENG ; Yuan Yuan ZHENG ; Yan Lin ZHANG ; Jian Lan XIE

Chinese Journal of Pathology 2023;52(6):592-598

7.Clinical and genetic characteristic in patients with disorders of sex development caused by Y chromosome copy number variant.

Jun Ke XIA ; Feng Yan TIAN ; Ya Qin HOU ; Yong Jiang ZHAO ; Xiang Dong KONG

Chinese Journal of Pediatrics 2023;61(5):459-463

8.Clinicopathological Features and Prognosis of Patients Newly Diagnosed With Lung Adenocarcinoma With Both EGFR Mutation and C-MET Amplification.

Wan-Ling WANG ; Cun-Bao XU ; Jin-Ling YANG ; Hong-Tu ZHANG ; Yi-Feng CHEN

Acta Academiae Medicinae Sinicae 2023;45(4):627-633

9.Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT.

Jiazhen CHANG ; Yingna SONG ; Qingwei QI ; Na HAO ; Juntao LIU

Chinese Journal of Medical Genetics 2023;40(8):922-927

10.Application of fluorescence in situ hybridization combined with chromosomal karyotyping analysis in children with disorders of sex development due to sex chromosome abnormalities.

Gaowei WANG ; Jin WANG ; Zhenhua ZHANG ; Rui LI ; Linfei LI ; Dongxiao LI ; Wancun ZHANG ; Yaodong ZHANG ; Meiye WANG

Chinese Journal of Medical Genetics 2023;40(8):947-953

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