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导致严重智力缺陷的基因变异 - 专区 - 生物谷
news.bioon.com
根据星期二发表于2007 年3月20 日The American Journal of Human Genetics电子版中的文章，研究人员辨认出一个新的基因突变，会导致与X染色体有关的智力缺陷，目前还没有分子技术可诊断这种智力缺陷。
MATH NEWS
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Volunteers must be prepared to provide a DNA sample (by a painless cheek swab). Interested readers should e-mail Uma Mallya: .uk Genetics and the link
Network Profiles
A systematic, large-scale resequencing screen of X-chromosome coding...
people.uea.ac.uk
... {Fatima E} and Srivastava, {Anand K} and James Cox and Ying Luo and Uma Mallya and Jenny Moon and Josef Parnau and Shehla Mohammed and Tolmie, ...
Education
A Genome Wide Association Study of Mathematical Ability Reveals an...
kclpure.kcl.ac.uk
Simon Baron-Cohen ; Laura Murphy ; Bhismadev Chakrabarti ; Ian Craig ; Uma Mallya ; Silvia Lakatosova ; Karola Rehnstrom ; Leena ...
Books & Literature
CiteULike: Mutations in the BRWD3 gene cause X-linked mental...
www.citeulike.org
... Gemma Buck, Jennifer Cole, Kristian Gray, Kelly Halliday, Katy Hills, Andrew Jenkinson, David Jones, Andrew Menzies, Tatiana Mironenko, Janet Perry, Keiran Raine, David Richardson, Rebecca Shepherd, Alexandra Small, Jennifer Varian, Sofie West, Sara Widaa, Uma Mallya, Richard Wooster, Jenny Moon, Ying Luo, ...
American Journal of Human Genetics Abstracts
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American Journal of Human Genetics Abstracts
Endrocrine Press
press.endocrine.org
Maternal Isodisomy for Chromosome 9 Causing Homozygosity for a Novel FOXE1 Mutation in Syndromic Congenital Hypothyroidism · The Journal of Clinical Endocrinology & Metabolism · Mireille Castanet, Uma Mallya, Maura Agostini, Erik Schoenmakers, Catherine Mitchell, Stephanie Demuth, F. Lucy ...
Geeks, Genes, and the Evolution of Asperger Syndrome
books.google.de
Warrier, Varun, Bhismadev Chakrabarti, Laura Murphy, Allen Chan, Ian Craig, Uma Mallya, Silvia Lakatošová, Karola Rehnstrom, Leena Peltonen, and Sally ...
Related Documents
CiteSeerX — A Genome Wide Association Study of Mathematical Ability...
citeseerx.ist.psu.edu
BibTeX @MISC{Baron-cohen_agenome, author = {Simon Baron-cohen and Laura Murphy and Bhismadev Chakrabarti and Ian Craig and Uma Mallya and Karola Rehnstrom …
Maternal isodisomy for a novel human FOXE1 gene mutation in syndromic...
www.endocrine-abstracts.org
Maternal isodisomy for a novel human FOXE1 gene mutation in syndromic congenital hypothyroidsim Mireille Castanet 1, Uma Mallya 2, Maura Agostini 1, Catherine ...
A Genome Wide Association Study of Mathematical Ability Reveals an...
www.scienceopen.com
A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: A Preliminary Study. Authors: Simon Baron-Cohen,,, Laura Murphy, Bhismadev Chakrabarti,, Ian Craig, Uma Mallya, Silvia Lakatošová, Karola ...
[PDF] British Human Genetics Conference Free Download PDF
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1 British Society for Human Genetics British Human Genetics Conference Monday-Wednesday, September University of Yo...
Scientific Publications
A Genome Wide Association Study of Mathematical Ability Reveals an...
www.ncbi.nlm.nih.gov
Simon Baron-Cohen,1,2,* Laura Murphy,1 Bhismadev Chakrabarti,1,3 Ian Craig,4Uma Mallya,1 Silvia Lakatošová,1 Karola Rehnstrom,5 Leena Peltonen,5 Sally Wheelwright,1 Carrie Allison,1 Simon E. Fisher,6,7 and Varun Warrier1,*. Momiao Xiong, Editor. 1Autism Research Centre, Department of ...
Genetic variant rs in the ARNT2 gene is associated with...
molecularautism.biomedcentral.com
... Sylvia Lakatosova, Sally Wheelwright, Carrie Allison, Uma Mallya, Alex Politt and Leena Peltonen for support at different points of the project.
X-linked Mental Retardation Type Raynaud - PMC - NCBI
www.ncbi.nlm.nih.gov
... Anand K Srivastava, James Cox, Ying Luo, Uma Mallya, Jenny Moon, Josef Parnau, Shehla Mohammed, John L Tolmie, Cheryl Shoubridge, ...
Genetic variation in the oxytocin receptor ( OXTR ) gene is...
molecularautism.biomedcentral.com
... Sally Wheelwright, Carrie Allison, Uma Mallya, Alex Politt, and the late Leena Peltonen for support at different stages of the project. Simon Fisher
Publications
Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor...
core.ac.uk
... Sofie West, Sara Widaa, Andy Yates, Rachael Catford, Julia Butler, Uma Mallya, Jenny Moon, Ying Luo, Huw Dorkins, Deborah Thompson, Douglas F. Easton ...
Genetic variant rs in the ARNT2 gene is associated with...
link.springer.com
Genetic variant rs in the ARNT2 gene is associated with Asperger Syndrome. Authors Sally Wheelwright, Carrie Allison, Uma Mallya, ...
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and...
www.wikidata.org
scientific article
Reports & Statements
Erratum: Corrigendum: Mutations in FRMD7 , a newly Nature
www.nature.com
Patrick Tarpey ,; Shery Thomas ,; Nagini Sarvananthan ,; Uma Mallya ,; Steven Lisgo ,; Chris J Talbot ,; Eryl O Roberts ,; Musarat Awan ,; Mylvaganam Surendran ...
A Musical Journey – Rekha Mallya
rekhamallya.wordpress.com
Uma Mallya says: May 15, at 6:28 pm. It was an excellent read Rekha , really proud of you . Keep up the good work ! Love and Regards .
Mutations in FRMD7 , a newly identified member of the FERM family,...
www.nature.com
Brief Communication
Hospitals | The Silicon City Bangalore (ಬೆಂಗಳೂರು)
siliconcitybangalore.wordpress.com
Uma Mallya Apollo Hospital, Vittal Mallya Road, Bangalore, 80) V Care Hospital & Pharma, No.29, 1st Mn Rd,1st Blk,hd Devegowda Rd, R T Nagar , ...
Miscellaneous
Michael Field, Patrick S - ppt download - SlidePlayerslideplayer.com › slide
slideplayer.com
... Keiran Raine, David Richardson, Rebecca Shepherd, Alexandra Small, Jennifer Varian, Sofie West, Sara Widaa, Uma Mallya, Richard Wooster, Jenny Moon, ...
FW: [AJHG-TOC] AJHG May (vol 80 no Groups
groups.yahoo.com
... Andrew Menzies, Janet Perry, Keiran Raine, Rebecca Shepherd, Alexandra Small, Jennifer Varian, Sara Widaa, Uma Mallya, Jenny Moon, ...
Uma Mallya Apollo Hospital - Bangalore | Karnataka
www.hospitalsdata.com
Uma Mallya Apollo Hospital - Bangalore, Karnataka, INDIA, latest news, latest articles.
Mallya - Names Encyclopedia
namespedia.com
Uma Mallya (1) Vishwanath Mallya (1) Mohandas Mallya (1) Sidhartha Mallya (1) Siddarth Mallya (1) Rohini Mallya (1) Shailesh Mallya (1) Sheshagiri Mallya (1)
The list for all aspects of biotechnology related to Indonesia ...
groups.yahoo.com
Yates, Rachael Catford, Julia Butler, Uma Mallya, Jenny Moon, Ying Luo, Huw Dorkins, Deborah Thompson, Douglas F. Easton, Richard ...
Uma Mallya
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resources, people, groups, collections, journals, conferences, series. Search. advanced search. ×. Search results for: Uma Mallya. Search for author's resources ...
Autistic Disorder: Mallya, Uma - Expertscape.com
expertscape.com
Medical and scientific articles about Autistic Disorder, written by Uma Mallya
Thyroid Diseases: Mallya, Uma - Expertscape.com
www.expertscape.com
Uma Mallya has special expertise in Thyroid Diseases
Epilepsy: Mallya, Uma - Expertscape.com
www.expertscape.com
Uma Mallya has special expertise in Epilepsy
A Genome Wide Association Study of Mathematical Ability ...
go.gale.com
Author(s): Simon Baron-Cohen 1 2 * , Laura Murphy 1 , Bhismadev Chakrabarti 13 , Ian Craig 4 , Uma Mallya 1 , Silvia Lakatosová 1 , Karola Rehnstrom
Altmetric – A systematic, large-scale resequencing screen of...
www.altmetric.com
Luo, Uma Mallya, Jenny Moon, Josef Parnau, Shehla Mohammed, John L Tolmie
, ...
Erratum: Mutations in FRMD7, a newly identified member of ...
mayoclinic.pure.elsevier.com
Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, Uma Mallya, Steven Lisgo, Chris J. Talbot, Eryl O. Roberts, Musarat Awan, Mylvaganam Surendran, ...
A Pooled Genome-Wide Association Study of Asperger Syndrome (pdf) |...
paperity.org
Paperity: the 1st multidisciplinary aggregator of Open Access journals & papers. Free fulltext PDF articles from hundreds of disciplines, all in one place
AUTISM RESEARCH CENTRE Section of Developmental Psychiatry at...
autism.boomja.com
The Autism Research section is dedicated to providing you with the best professional information resources available on research related to autism spectrum...
BooKsc Proxy Mirror - Gecz: free download. Ebooks library. On-line ...
booksc.bypassed.eu
... Jonathon Hinton, David Jones, Andrew Menzies, Tatiana Mironenko, Janet Perry, Keiran Raine, David Richardson, Rebecca Shepherd, Alexandra Small, Calli Tofts, Jennifer Varian, Sofie West, Sara Widaa, Andy Yates, Rachael Catford, Julia Butler, Uma Mallya, Jenny Moon, Ying Luo, Huw Dorkins, Deborah Thompson, ...
A systematic, large-scale resequencing screen of X-chromosome coding...
www.scholars.northwestern.edu
... Fatima E. Abidi, Anand K. Srivastava, James Cox, Ying Luo, Uma Mallya, Jenny Moon, Josef Parnau, Shehla Mohammed, John L. Tolmie, Cheryl Shoubridge, ...
A Pooled Genome-Wide Association Study of Asperger Syndrome | Read by...
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A Pooled Genome-Wide Association Study of Asperger Syndrome. Varun Warrier, Bhismadev Chakrabarti, Laura Murphy, Allen Chan, Ian Craig, Uma Mallya, ...
Hospitals in Bangalore: List of Hospitals and Clinicswww.bangalorecircle.com › pages › DIR › Hospitals
www.bangalorecircle.com
Uma Mallya Apollo Hospital, Vittal Mallya Road, Bangalore, 80) V Care Hospital & Pharma, No.29, 1st Mn Rd,1st Blk,hd Devegowda Rd, R T Nagar , ...
Mutations in the DLG3 gene cause nonsyndromic X-linked mental...
www.sigmaaldrich.com
Sigma-Aldrich offers abstracts and full-text articles by [Patrick Tarpey, Josep Parnau, Matthew Blow, Hayley Woffendin, Graham Bignell, Charles Cox, James Cox,...
A Pooled Genome-Wide Association Study of Asperger Syndrome
journals.plos.org
Asperger Syndrome (AS) is a neurodevelopmental condition characterized by impairments in social interaction and communication, ... Uma Mallya, Silvia Lakatošová,
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