Cargando…

Molecular and Cytogenetic Characterization of a Fetus with Mosaic Ring Chromosome 13: A Very Rare Case

Detalles Bibliográficos
Autores principales:	Zhao, Xin-Rong, Han, Xu, Wang, Yan-Lin, Hu, Wen-Jing
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Clinical Challenge
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742933/ https://www.ncbi.nlm.nih.gov/pubmed/29237938 http://dx.doi.org/10.4103/0366-6999.220308

Ejemplares similares

Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7
por: Tsai, Li-Ping, et al.
Publicado: (2011)

Wernicke Encephalopathy in a Patient with Pulmonary and Abdominal Tuberculosis
por: Gan, Yun-Cui, et al.
Publicado: (2017)

Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome
por: Luo, Hunjin, et al.
Publicado: (2022)

Clinical, cytogenetic and molecular study of a case of ring chromosome 10
por: Čiuladaitė, Živilė, et al.
Publicado: (2015)

Crossover transseptal vasovasostomy: alternative for very selected cases of iatrogenic injury to vas deferens
por: Korkes, Fernando, et al.
Publicado: (2019)

Molecular cytogenetic characterization of a mosaic small supernumerary marker chromosome derived from chromosome Y in an azoospermic male: A case report
por: Zhang, Hongguo, et al.
Publicado: (2019)

An Improved Urethral Catheterization in Female Pigs: A Pilot Study
por: Li, Da-Peng, et al.
Publicado: (2017)

Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome
por: Petter, Cristian, et al.
Publicado: (2019)

Mosaic Ring Chromosome 13 Presented with Isolated Male Infertility: Case Report
por: Zamanian, Mohammadreza, et al.
Publicado: (2023)

Molecular cytogenetic characterization of a de novo derivative chromosome X with an unbalanced t(X;9) translocation in a fetus and literature review
por: Wu, Qiong, et al.
Publicado: (2022)

Puzzle and Challenge in Differentiating Immunoglobulin G4-related Cholangitis from Hilar Cholangiocarcinoma
por: Hu, Hai-Jie, et al.
Publicado: (2017)

Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies
por: Basaran, Seher, et al.
Publicado: (2022)

A Novel Mutation of Notch homolog protein 2 gene in a Chinese Family with Hajdu-Cheney Syndrome
por: Gong, Ruo-Lan, et al.
Publicado: (2017)

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray
por: Yao, Tien-Yu, et al.
Publicado: (2021)

Induction of Anesthesia with Dexmedetomidine and Sevoflurane for a Pediatric Difficult Airway
por: Wei, Ling-Xin, et al.
Publicado: (2017)

Characterization of a very rare case of living ewe-buck hybrid using classical and molecular cytogenetics
por: Pauciullo, Alfredo, et al.
Publicado: (2016)

An Infant with Abernethy Malformation Associated with Heterotaxy and Pulmonary Hypertension
por: Zhang, Xiao-Lin, et al.
Publicado: (2017)

Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management
por: Aw, Lin Da, et al.
Publicado: (2016)

Treatment for 15 Cases of Cervical Tuberculosis
por: Yao, Min, et al.
Publicado: (2017)

Testicular calculus: A rare case
por: Sen, Volkan, et al.
Publicado: (2015)

Thyrotoxicosis Occurring in Secondary Hyperparathyroidism Patients Undergoing Dialysis after Total Parathyroidectomy with Autotransplantation
por: Xu, Zhou, et al.
Publicado: (2017)

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2
por: Li, Meihua, et al.
Publicado: (2022)

Clinical and molecular cytogenetic findings and pregnancy outcomes of fetuses with isochromosome Y
por: He, Yiqun, et al.
Publicado: (2022)

Mosaicism of Tetrasomy 18p: Clinical and Cytogenetic Findings in a Female Child
por: Bai, Jin-Li, et al.
Publicado: (2017)

Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods
por: Omori Sarabi, Sadaf, et al.
Publicado: (2020)

Rare but unforgettable cause of hypotension
por: Marinho, Ana Vera Vera, et al.
Publicado: (2020)

A complicated true sliding hernia presenting as a spontaneous enteroscrotal fistula in an adult
por: Rajamanickam, Saravana, et al.
Publicado: (2010)

Traumatic brain injury complicated by environmental hyperthermia
por: Hermstad, Erik, et al.
Publicado: (2010)

Cerebriform plaque on the scalp
por: Betsy, Ambooken, et al.
Publicado: (2012)

Elevated Yellow Nodule over the Scalp in a Middle-aged Man
por: Anand, Mani, et al.
Publicado: (2011)

A Woman with Recent Jaundice and Pruritus
por: Behnava, Bita, et al.
Publicado: (2010)

Difficult nasoendotracheal intubation in a patient with severe maxillofacial trauma
por: Mesgarzadeh, Ali Hossein, et al.
Publicado: (2012)

Spangled Hair in Siblings
por: Murugusundram, Sundaram
Publicado: (2009)

Itchy Black Hair Bristles on Back
por: Gutte, Rameshwar M
Publicado: (2012)

Traumatic bilateral carotid and vertebral artery dissection
por: Koleilat, Issam, et al.
Publicado: (2014)

Pink Nodule with a Peculiar Pattern on Trichoscopy
por: Ankad, Balachandra S, et al.
Publicado: (2013)

Multiple Firm Mobile Swellings Over The Scalp
por: Adya, Keshavmurthy A, et al.
Publicado: (2012)

A Solitary Asymptomatic Tumor on the Knee
por: Monia, Youssef, et al.
Publicado: (2015)

Vitiliginous Alopecia Masquerading as Frontal Fibrosing Alopecia
por: Pigem, Ramon, et al.
Publicado: (2015)

A 14-year-old Boy with an Irregularly Bordered, Erythematous, Alopecic Patch of the Scalp
por: Iorizzo, Matilde, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_4brg7gv8nm5pg9hg921saa0r9i