DiGeorge syndrome

Results: 104



#Item
1RIMD–IPR Joint Seminar “Insight into the functions of the CRK gene family from a view of DiGeorge Syndrome” Akira Imamoto D.D.S., Ph.D. The University of Chicago

RIMD–IPR Joint Seminar “Insight into the functions of the CRK gene family from a view of DiGeorge Syndrome” Akira Imamoto D.D.S., Ph.D. The University of Chicago

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Source URL: www.med.osaka-u.ac.jp

Language: English - Date: 2017-03-29 04:48:17
    2®  What is NACE Plus ? NACE Plus® has the same characteristics as the NACE® test , but is an extended version that also incorporates the detection of chromosome 9 and 16 trisomies, which are closely related with

    ® What is NACE Plus ? NACE Plus® has the same characteristics as the NACE® test , but is an extended version that also incorporates the detection of chromosome 9 and 16 trisomies, which are closely related with

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    Source URL: www.igenomix.ae

    Language: English - Date: 2015-02-24 12:47:41
    3Clinical and Molecular Cytogenetics Laboratory DEPARTMENT OF PATHOLOGY UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER, SAN ANTONIO CLIA# 45D0660483 CAP# Room 318C, 7703 Floyd Curl Drive, San Antonio, TXPho

    Clinical and Molecular Cytogenetics Laboratory DEPARTMENT OF PATHOLOGY UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER, SAN ANTONIO CLIA# 45D0660483 CAP# Room 318C, 7703 Floyd Curl Drive, San Antonio, TXPho

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    Source URL: pathology.uthscsa.edu

    Language: English - Date: 2014-08-11 09:35:37
    4ECHO Adult study  ECHO study is a research group based at Cardiff University that wants to find out more about the life course and health of individuals with genetic syndromes. We are currently looking to hear from ad

    ECHO Adult study  ECHO study is a research group based at Cardiff University that wants to find out more about the life course and health of individuals with genetic syndromes. We are currently looking to hear from ad

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    Source URL: rarechromo.org

    Language: English - Date: 2016-06-07 05:42:50
    5ABOUT C22C Chromosome 22 was the first chromosome to be sequenced in the Human Genome Project. Beyond the conditions listed in this brochure, chromosome 22 has also been researched as a link to bi-polar disorder, schizop

    ABOUT C22C Chromosome 22 was the first chromosome to be sequenced in the Human Genome Project. Beyond the conditions listed in this brochure, chromosome 22 has also been researched as a link to bi-polar disorder, schizop

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    Source URL: www.c22c.org

    Language: English - Date: 2014-01-07 21:00:04
    6July, 24, 2013 Dear Friend: On behalf of the Board and committed athletes of 22k for 22q, I would like to thank you for taking the time to read and consider this sponsorship proposal. 22k for 22q is both a fundraising an

    July, 24, 2013 Dear Friend: On behalf of the Board and committed athletes of 22k for 22q, I would like to thank you for taking the time to read and consider this sponsorship proposal. 22k for 22q is both a fundraising an

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    Source URL: www.22q.org

    Language: English - Date: 2013-08-12 13:45:47
    7ABOUT C22C Chromosome 22 was the first chromosome to be sequenced in the Human Genome Project. Beyond the conditions listed in this brochure, chromosome 22 has also been researched as a link to bi-polar disorder, schizop

    ABOUT C22C Chromosome 22 was the first chromosome to be sequenced in the Human Genome Project. Beyond the conditions listed in this brochure, chromosome 22 has also been researched as a link to bi-polar disorder, schizop

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    Source URL: c22c.org

    Language: English - Date: 2014-01-07 21:00:04
    8The Unique Garden at Hampton Court Palace Flower Show 2015 Sponsor A Plant Appeal We would like to thank the following people for their extremely kind donations, to sponsor a plant for the Unique Garden at the Hampton Co

    The Unique Garden at Hampton Court Palace Flower Show 2015 Sponsor A Plant Appeal We would like to thank the following people for their extremely kind donations, to sponsor a plant for the Unique Garden at the Hampton Co

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    Source URL: www.rarechromo.org

    Language: English - Date: 2015-05-15 10:47:17
    9   The Journal of Rare Disorders PRENATAL FINDINGS IN CASES OF FAMILIAL AND SPORADIC 22Q11.2 DELETION  SYNDROME (DIGEORGE SYNDROME/VELOCARDIOFACIAL SYNDROME) 

      The Journal of Rare Disorders PRENATAL FINDINGS IN CASES OF FAMILIAL AND SPORADIC 22Q11.2 DELETION  SYNDROME (DIGEORGE SYNDROME/VELOCARDIOFACIAL SYNDROME) 

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    Source URL: www.journalofraredisorders.com

    Language: English - Date: 2013-04-14 19:58:58
    10Velo-Cardio-Facial Syndrome Alternative names 22q11.2 deletion syndrome, Sedlackova syndrome, DiGeorge syndrome, Shprintzen syndrome, Conotruncal anomaly face syndrome. Genetics / aetiology 85-90% of individuals with VCF

    Velo-Cardio-Facial Syndrome Alternative names 22q11.2 deletion syndrome, Sedlackova syndrome, DiGeorge syndrome, Shprintzen syndrome, Conotruncal anomaly face syndrome. Genetics / aetiology 85-90% of individuals with VCF

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    Source URL: www.ssbp.org.uk

    Language: English - Date: 2015-05-13 15:34:18