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Female X-linked Alport syndrome with somatic mosaicism. [electronic resource] by
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- Nozu, Kandai
- Minamikawa, Shogo
- Yamamura, Tomohiko
- Nakanishi, Keita
- Kaneda, Hisashi
- Hamada, Riku
- Nozu, Yoshimi
- Shono, Akemi
- Ninchoji, Takeshi
- Morisada, Naoya
- Ishimori, Shingo
- Fujimura, Junya
- Horinouchi, Tomoko
- Kaito, Hiroshi
- Nakanishi, Koichi
- Morioka, Ichiro
- Taniguchi-Ikeda, Mariko
- Iijima, Kazumoto
Producer: 20180611
In:
Clinical and experimental nephrology vol. 21
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None [electronic resource] by
- Johnston, Jennifer J
- Williamson, Kathleen A
- Chou, Christopher M
- Sapp, Julie C
- Ansari, Morad
- Chapman, Heather M
- Cooper, David N
- Dabir, Tabib
- Dudley, Jeffrey N
- Holt, Richard J
- Ragge, Nicola K
- Schäffer, Alejandro A
- Sen, Shurjo K
- Slavotinek, Anne M
- FitzPatrick, David R
- Glaser, Thomas M
- Stewart, Fiona
- Black, Graeme Cm
- Biesecker, Leslie G
Producer: 20200603
In:
Journal of medical genetics vol. 56
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Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis. [electronic resource] by
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- Nandini, Adayapalam
- Woods, Rickie G
- Fairbairn, David J
- Rowell, John A
- Young, David
- Susman, Rachel D
- Brown, Simon A
- Hyland, Valentine J
- Robertson, Jeremy D
Producer: 20181017
In:
Molecular genetics & genomic medicine vol. 6
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MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients. [electronic resource] by
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- Oliveira, Guiomar
- Katz, Cécile
- Feng, Jinong
- Yan, Jin
- Yang, Chunmei
- Marques, Carla
- Ataíde, Assunção
- Miguel, Teresa S
- Borges, Luís
- Almeida, Joana
- Correia, Catarina
- Currais, António
- Bento, Celeste
- Mota-Vieira, Luísa
- Temudo, Teresa
- Santos, Mónica
- Maciel, Patrícia
- Sommer, Steve S
- Vicente, Astrid M
Producer: 20070814
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 144B
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MicroRNA regulation of Cbx7 mediates a switch of Polycomb orthologs during ESC differentiation. [electronic resource] by
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- Wu, Hsan-Au
- Banito, Ana
- Kunowska, Natalia
- Racek, Tomas
- Pemberton, Helen N
- Beolchi, Patrizia
- Lavial, Fabrice
- Masui, Osamu
- Vermeulen, Michiel
- Carroll, Thomas
- Graumann, Johannes
- Heard, Edith
- Dillon, Niall
- Azuara, Veronique
- Snijders, Ambrosius P
- Peters, Gordon
- Bernstein, Emily
- Gil, Jesus
Producer: 20120501
In:
Cell stem cell vol. 10
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Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. [electronic resource] by
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- Peters, Sarika U
- Tavyev, Y Jane
- Zhang, Feng
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- Schaaf, Christian P
- Richman, Ronald
- Fang, Ping
- Glaze, Daniel G
- Lupski, James R
- Zoghbi, Huda Y
Producer: 20100118
In:
Annals of neurology vol. 66
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Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease. [electronic resource] by
- Wu, Hao
- Luo, Junjie
- Yu, Huimin
- Rattner, Amir
- Mo, Alisa
- Wang, Yanshu
- Smallwood, Philip M
- Erlanger, Bracha
- Wheelan, Sarah J
- Nathans, Jeremy
Producer: 20140307
In:
Neuron vol. 81
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Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis. [electronic resource] by
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- Onat, Onur E
- Balandraud, Nathalie
- Martin, Gabriel V
- Nelson, J Lee
- Azzouz, Doua F
- Auger, Isabelle
- Arnoux, Fanny
- Martin, Marielle
- Roudier, Jean
- Ozcelik, Tayfun
- Lambert, Nathalie C
Producer: 20170719
In:
PloS one vol. 11
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1579.
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Derivation and differentiation of haploid human embryonic stem cells. [electronic resource] by
- Sagi, Ido
- Chia, Gloryn
- Golan-Lev, Tamar
- Peretz, Mordecai
- Weissbein, Uri
- Sui, Lina
- Sauer, Mark V
- Yanuka, Ofra
- Egli, Dieter
- Benvenisty, Nissim
Producer: 20160510
In:
Nature vol. 532
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