8.6 Karyotypes and Chromosomal Disorders

8.6 Karyotypes and Chromosomal Disorders

Video Analysis for 8.6 Karyotypes and Chromosomal Disorders

May 13, 2014

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8.6 Karyotypes and Chromosomal Disorders

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  • www.youtube.com   Karyotypes - YouTube

    Mar 01, 2012 · This video will answer the following questions: What is a karyotype? What three things can a karyotype tell a biologist? What's the difference between an ...

    http://www.youtube.com/watch?v=hNMYV213xu0

  • www.youtube.com   Chromosomal Structure & Human Karyotype - YouTube

    Jan 23, 2012 · Mr. Lima describes the basic stucture of the eukaryotic chromosomes (with focus on human chromosomes) and explains the normal human karyotype (including ...

    http://www.youtube.com/watch?v=JQENxZrLQ9s

  • en.wikipedia.org   Chromosome - Wikipedia, the free encyclopedia

    The word chromosome comes from the Greek χρῶμα (chroma, "colour") and σῶμα (soma, "body"). Chromatin and chromosomes are both very strongly stained by ...

    https://en.wikipedia.org/wiki/Chromosome

  • www.glowm.com   Genetic and Nongenetic Causes of Pregnancy Loss | GLOWM

    A large proportion of embryos never implant, and many that do are lost without clinical recognition of pregnancy. Pregnancy losses are repetitive.

    http://www.glowm.com/section_view/heading/Genetic%20and%20Nongenetic%20Causes%20of%20Pregnancy%20Loss/item/318

  • www.aetna.com   Recurrent Pregnancy Loss - Aetna

    Karyotype of abortus tissue when a couple with recurrent pregnancy loss experiences a subsequent spontaneous abortion;

    http://www.aetna.com/cpb/medical/data/300_399/0348.html

  • www.intechopen.com   Increased Fetal Nuchal Translucency Thickness and Normal ...

    Increased Fetal Nuchal Translucency Thickness and Normal Karyotype: Prenatal and Postnatal Outcome

    http://www.intechopen.com/books/down-syndrome/increased-fetal-nuchal-translucency-thickness-and-normal-karyotype-prenatal-and-postnatal-outcome

  • en.wikipedia.org   Centromere - Wikipedia, the free encyclopedia

    The centromere is the part of a chromosome that links sister chromatids. During mitosis, spindle fibers attach to the centromere via the kinetochore. [1]

    https://en.wikipedia.org/wiki/Centromere

  • www.aetna.com   Infertility - Aetna

    Number: 0327. Policy. Notes: For purposes of this entire policy, Aetna covers diagnostic infertility services to determine the cause of infertility and treatment only ...

    http://www.aetna.com/cpb/medical/data/300_399/0327.html

  • www.science.gov   mosaic turner syndrome: Topics by Science.gov

    syndrome could help identifying females with rapid growth of aortic diameter, and may enhance clinical decision-making based on serial CMR. PMID:23742092

    http://www.science.gov/topicpages/m/mosaic+turner+syndrome.html

  • www.flashcardmachine.com   Biology Flashcards - Flashcard Machine - Create, Study and ...

    Flashcard Machine - create, study and share online flash cards ― ― ― My Flashcards; Flashcard Library; About; Contribute; Search; Help; Sign In; Create Account

    http://www.flashcardmachine.com/biology.html

  • www.inchem.org   Benzene (EHC 150, 1993) - INCHEM

    INTERNATIONAL PROGRAMME ON CHEMICAL SAFETY ENVIRONMENTAL HEALTH CRITERIA 150 BENZENE This report contains the collective views of an international …

    http://www.inchem.org/documents/ehc/ehc/ehc150.htm

  • www.ijpeonline.com   Growth hormone significantly increases the adult height of ...

    Open Badges Research Growth hormone significantly increases the adult height of children with idiopathic short stature: comparison of subgroups and benefit

    http://www.ijpeonline.com/content/2014/1/15

  • omim.org   OMIM Entry - # 104300 - ALZHEIMER DISEASE; AD

    #104300 icd+ snomedct: 26929004 ...

    http://omim.org/entry/104300

  • www.science.gov   patients significantly increased: Topics by Science.gov

    Sample records for patients significantly increased ».?... « ...

    http://www.science.gov/topicpages/p/patients+significantly+increased.html

  • www.ufrgs.br   Hematopoietic stem cell transplantation (HSCT)

    Laughlin et al ref: Sanz et al ref: Rocha et al ref (Rocha V, Arcese W, Sanz G, et al. Prognostic factors of outcome after unrelated cord blood transplant (UCBT) in ...

    http://www.ufrgs.br/imunovet/molecular_immunology/grafts_HSCT.html

  • www.recherchecliniquepariscentre.fr   Publications | Recherche Clinique Paris Descartes Necker ...

    Année Publication Lien PubMed; 2015: Efficacy and safety of tocilizumab in patients with polyarticular-course juvenile idiopathic arthritis: results from a phase 3 ...

    http://www.recherchecliniquepariscentre.fr/?page_id=41

  • www.doctortipster.com   Klinefelter Syndrome Causes, Symptoms And Karyotype

    Klinefelter syndrome ... intellectual disorders. Each additional X chromosome, reduces the coefficient of intelligence with 15-16 points, language being the most affected. About 15% of cases of Klinefelter syndrome, presents mosaic karyotype and have ...

    Doctor Tipster   •   6 years ago

    http://www.doctortipster.com/3314-klinefelter-syndrome.html

  • www.medscape.com   Chromosomal Microarray Analysis OK for Prenatal Diagnosis

    The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine have issued guidelines on the use of chromosomal microarray analysis ... or autism spectrum disorders but have normal karyotypes. A variation of CMA ...

    Medscape News   •   4 years ago

    http://www.medscape.com/viewarticle/814831

  • www.thebridgeportnews.com   Health Notes: Week of Nov. 30

    Royce York, director of Respiratory Services at Griffin Hospital, will present “Sleep Well, Be Well” a discussion about the medical definition of sleep, sleep disorders and treatments ... the holidays Tuesday, Dec. 8, 6 …

    thebridgeportnews.com   •   2 years ago

    http://www.thebridgeportnews.com/17415/health-notes-week-of-nov-30/

  • www.ncbi.nlm.nih.gov   47,XYY karyotypes and pervasive developmental disorders.

    nicolson@box-n.nih.gov OBJECTIVE: The presence of a 47, XYY karyotype in boys with pervasive developmental disorders (PDDs) has rarely been described in the past. Herein, 2 boys with PDDs and a supernumerary Y chromosome are presented.

    ncbi.nlm.nih.gov   •   4 years ago

    http://www.ncbi.nlm.nih.gov/pubmed/9729690

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