Cargando…

Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism

Detalles Bibliográficos
Autores principales:	Grzesiuk, Juliana Dourado, Pereira, Ciro Silveira, Grangeiro, Carlos Henrique Paiva, Picanço-Albuquerque, Clarissa Gondim, Oliveira-Gennaro, Flávia Gaona, Machado, Filipe Brum, Medina-Acosta, Enrique, Ramos, Ester Silveira, Yoshimoto, Maisa, Martelli, Lucia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932718/ https://www.ncbi.nlm.nih.gov/pubmed/27382416 http://dx.doi.org/10.1186/s13039-016-0262-8

Ejemplares similares

Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism
por: Grzesiuk, Juliana Dourado, et al.
Publicado: (2016)

Autism Spectrum Disorder in a Girl with a De Novo X;19 Balanced Translocation
por: Baruffi, Marcelo Razera, et al.
Publicado: (2012)

Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
por: Carvalho, Simone da Costa e Silva, et al.
Publicado: (2018)

High frequency of Y chromosome microdeletions in male infertility patients with 45,X/46,XY mosaicism
por: Li, Leilei, et al.
Publicado: (2020)

The X chromosome and male infertility
por: Vockel, Matthias, et al.
Publicado: (2019)

Unbalanced X chromosome mosaicism in B cells of mice with X-linked immunodeficiency
Publicado: (1983)

Choroideremia associated with an X-autosomal translocation
por: Siu, Victoria M., et al.
Publicado: (1990)

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
por: Machiela, Mitchell J., et al.
Publicado: (2016)

Non-mosaic X monosomy (77,X) in a female dog with signs of virilization
por: Szczerbal, Izabela, et al.
Publicado: (2022)

Mosaic Turner Syndrome With 45,X/46,XY Mosaicism and Apparent Absent Uterus
por: Alhajjaj, Alya, et al.
Publicado: (2021)

Germline mosaicism in X-linked periventricular nodular heterotopia
por: LaPointe, Monique M, et al.
Publicado: (2014)

Intranuclear inclusions in a fragile X mosaic male
por: Pretto, Dalyir I, et al.
Publicado: (2013)

45,X/47,XXX Mosaicism and Short Stature
por: Everest, Erica, et al.
Publicado: (2015)

Educational Case: Fragile X Syndrome with Size Mosaicism
por: Geisler, Daniel
Publicado: (2019)

Reciprocal X;1 translocation in a calf
por: Mayr, B, et al.
Publicado: (1998)

A rare case of mixed gonadal dysgenesis with mosaicism 45, X/46, X, +mar
por: Soheilipour, Fahimeh, et al.
Publicado: (2014)

Prenatal Diagnosis of Placental Mesenchymal Dysplasia with 46, X, Isochromosome Xq/45, X Mosaicism
por: Hsu, Chin-Chieh, et al.
Publicado: (2022)

Mild phenotypes associated with an unbalanced X‐autosome translocation, 46,X,der(X)t(X;8)(q28;q13)
por: Watanabe, Takafumi, et al.
Publicado: (2018)

Hypothenar hammer syndrome: case report and literature review()
por: Queiroz, Márcia Maria Muniz de, et al.
Publicado: (2013)

Mosaic triple X syndrome in a female with primary amenorrhea
por: Venkateshwari, A., et al.
Publicado: (2012)

5(me)CpG Epigenetic Marks Neighboring a Primate-Conserved Core Promoter Short Tandem Repeat Indicate X-Chromosome Inactivation
por: Machado, Filipe Brum, et al.
Publicado: (2014)

Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients
por: Shen, Ming-Ching, et al.
Publicado: (2022)

Cardiovascular Pathology in Males and Females with 45,X/46,XY Mosaicism
por: De Groote, Katya, et al.
Publicado: (2013)

Somatic Mosaicism in a Male Patient With X-linked Alport Syndrome
por: Bu, Lihong, et al.
Publicado: (2019)

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
por: Baker, Emma K., et al.
Publicado: (2019)

Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes
por: Zhou, Weiyin, et al.
Publicado: (2021)

Searching chromosome mosaicisms in 45,X Turner syndrome: how relevant is it?
por: Soares, Jéssica Silva, et al.
Publicado: (2021)

Premature ovarian aging in primary infertility: Triple X syndrome
por: Kodandapani, Sreelakshmi, et al.
Publicado: (2011)

An Infertile Azoospermic Male With 45, X T(Yp;15) Karyotype
por: Abiri, Maryam, et al.
Publicado: (2021)

Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement
por: Shchelochkov, Oleg A, et al.
Publicado: (2008)

Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome
por: Mailick, Marsha R., et al.
Publicado: (2018)

X-autosome and X-Y Translocations in Female Carriers: X-chromosome Inactivation Easily Detectable by 5-ethynyl-2-deoxyuridine (EdU)
por: Donat, M, et al.
Publicado: (2017)

Kallmann Syndrome and X-linked Ichthyosis Caused by Translocation Between Chromosomes X and Y: A Case Report
por: Sait, Haseena, et al.
Publicado: (2021)

45,X mosaicism in northeast China: a clinical report and review of the literature
por: Liu, Xiang-Yin, et al.
Publicado: (2013)

Extra X Chromosome in Mosaic Klinefelter Syndrome Is Associated with a Hematologic Malignancy
por: Jang, Mi-Ae, et al.
Publicado: (2013)

45,X/46,XY Mosaicism and Normozoospermia in a Patient with Male Phenotype
por: Ketheeswaran, Shathmigha, et al.
Publicado: (2019)

Ventajas y desventajas del colon x enema simple vs doble contraste
por: Gaona Chávez, César
Publicado: (2003)

Random X Inactivation and Extensive Mosaicism in Human Placenta Revealed by Analysis of Allele-Specific Gene Expression along the X Chromosome
por: Moreira de Mello, Joana Carvalho, et al.
Publicado: (2010)

Male Infertility in Robertsonian Translocation: A Case Report
por: Almesned, Razan K., et al.
Publicado: (2020)

MiT translocation renal cell carcinomas: two subgroups of tumours with translocations involving 6p21 [t (6; 11)] and Xp11.2 [t (X;1 or X or 17)]
por: Hora, Milan, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_p9t28rbgl98ardf96fuiu18v84