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         Jacobsen Syndrome:     more detail
  1. Asperger Syndrome and Psychotherapy: Understanding Asperger Perspectives by Paula Jacobsen, 2003-03
  2. Jacobsen syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Dawn, MS, CGC Cardeiro, 2005
  3. Understanding How Asperger Children and Adolescents Think and Learn: Creating Manageable Environments for AS Students by Paula Jacobsen, 2005-06-15

41. Medicalseek - Search Engine For The Healthcare Industry
Conditions and DiseasesRare Disordersjacobsen syndrome Danny's 11q InformationPage A mother shares her story about having a son with jacobsen syndrome.
http://www.medicalseek.net/Conditions_and_Diseases_Rare_Disorders_Jacobsen_Syndr
CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Rare Disorders Jacobsen Syndrome
Conditions and Diseases:Rare Disorders:Jacobsen Syndrome

  • Danny's 11q Information Page
    A mother shares her story about having a son with Jacobsen Syndrome.
    hometown.aol.com/deidran/danny.html
    Institute of Child Health

    An article with an explanation of Jacobsen Syndrome.
    ich.ucl.ac.uk/units/mhu/fws/frames/jsof...
    NORD - Jacobsen Syndrome

    A look at the alternate names, a general discussion and resources.
    stepstn.com/cgi-win/nord.exe?proc=Redir... The Fragile WEB Site Information on Jacobsen syndrome, the chromosome deletion syndrome, for the families and carers of JS patients. Reference databaase, family support groups and clinical information. web.ukonline.co.uk/c.jones/contents.htm
CATEGORIES ADD A LINK ADVERTISE CONTACT US ... FORUMS

42. WebMD -
JA Jackknife Convulsion nord Jackson Weiss Syndrome nord JacksonWeiss Craniosynostosisnord jacobsen syndrome nord JACS (Jewish Alcoholics, Chemically
http://my.webmd.com/content/healthwise/152/37747.htm

43. THE LIGHTNING HYPERTEXT OF DISEASE.
NONMEMBER SEARCH JBS Packet No. 1 24374 jacobsen syndrome =jbs 11q-deletionsyndrome partial 11q monosomy syndrome key words terminology, JB
http://www.pathinfo.com/cgi-bin/lh.cgi?tx=jbs

44. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : J Diseases Da
J waves Jabs syndrome see Blau syndrome Jaccoud's arthropathy JacksonWeiss syndromejacobsen syndrome Jadassohn nevus phakomatosis see Epidermal naevus
http://www.diseasesdatabase.com/sieve/disease_index_j.asp
Diseases Database [Previous page] [Search] [Index] [Feedback]
Diseases Database disease, symptom, sign, etc alphabetical index : J
J waves
Jabs syndrome see Blau syndrome
Jaccoud's arthropathy

Jackson-Lawler congenital pachyonychia

Jackson-Weiss syndrome
...
Jacobsen syndrome

Jadassohn nevus phakomatosis see Epidermal naevus syndrome
Jadassohn-Dösseker disease see Pretibial myxoedema
Jadassohn-Lewandowsky syndrome

Jaeken syndrome see Carbohydrate deficient glycoprotein syndrome type 1a
Jaffe-Campanacci syndrome
Jaffe-Lichtenstein syndrome Jakob-Creutzfeldt Disease Jansky-Bielschowsky disease see Ceroid lipofuscinosis neuronal 2 late infantile Janz juvenile myoclonic epilepsy Japanese encephalitis Japanese river fever see Scrub typhus Jarcho-Levin syndrome Jaundice Jaundice of prematurity Jaw muscle spasm see Trismus Jaw protrusion see Prognathia Jaw small see Micrognathia Jaw-winking syndrome JC virus Jellyfish sting ... Jensen syndrome Jerky pulse see Rapid up-stroke pulse Jervell and Lange Nielsen syndrome see Lange Nielsen syndrome Jet lag Jeune's thoracic dystrophy syndrome Jiggers see Tungiasis Job's syndrome see Hyperimmunoglobulin E (IgE) syndrome Jock itch see Tinea cruris Jod-Basedow thyrotoxicosis Johanson-Blizzard syndrome Joint contracture see Contractures Joint effusion see Arthropathy Joint hyperextensibility see Joint hypermobility Joint hypermobility Joint infection (direct) see Septic arthropathy Joint laxity see Joint hypermobility Joint pain or swelling or disorder see Arthropathy Joubert syndrome Joubert-Boltshauser syndrome see Joubert syndrome Jugular paraganglioma

45. Service Page - Pathologie Information
Translate this page MALADIE jacobsen syndrome de, MIM 147791, Autre(s) site(s) Internet(4), Type(s) de consultations adaptées. Conseil génétique.
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=2308

46. Syndrome DB - Table Of Contents
J. jackknife spasm JacksonWeiss syndrome (JWS) jacobsen syndrome (JBS) Jadassohnnevus phakomatosis (JNP) Jaeken syndrome Jaffe-Campanacci syndrome Jahnke
http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_j.html
Multiple Congenital Anomaly/Mental Retardation Syndromes
Table of Contents
Return to Entry Page
A
B C ... Z
J
jackknife spasm
Jackson-Weiss syndrome (JWS)

Jacobsen syndrome (JBS)

Jadassohn nevus phakomatosis (JNP)
...
U.S. National Library of Medicine
, 8600 Rockville Pike, Bethesda, MD 20894
National Institutes of Health

Privacy
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Last updated: 20 November 2001

47. I
Isaac's Syndrome ( Fasciculation). Ischemic Attack, Transient (TIA). IvemarkSyndrome. J. jacobsen syndrome Jaundice. Jaundice, Neonatal. Job's Syndrome. K.
http://www.mashhadkit.com/iranmedicine/diseases-list/diseases-i-j-k-l.htm
I
Ichthyosis IgA Nephropathy Ileus Immersion Foot ... Infertility (.. Male Genital Diseases) Infertility (Female Genital Diseases ..) Inflammation Inflammatory Bowel Diseases Influenza Injury ... Ivemark Syndrome
J
Jacobsen Syndrome Jaundice Jaundice, Neonatal Job's Syndrome
K
Kabuki Make-Up Syndrome Kala Azar Kallmann Syndrome Kartagener Syndrome ... Kwashiorkor
L
Labyrinth Diseases Labyrinthitis Lacrimal Duct Obstruction Lactation Disorders ... Larsen Syndrome (not on MeSH) Larva Migrans Laryngeal Neoplasms Laryngitis Laryngomalacia ... Lysosomal Storage Diseases

48. Page Neonatal Diseases And Disorders
Back to top of Page. jacobsen syndrome. of Child Health (UK) About jacobsen syndromeOMIM; McKusik NCBI (US) The Int'l 11;22 Translocation Network
http://www.insight-media.co.uk/users/stevew/Pages/Page Neonatal Diseases and Dis
PAGE NEONATAL DISEASES AND DISORDERS
General, Neonatal Diseases and Disorders
Rubinstein-Taybi Syndrome
Abnormalities Smith-Lemli-Opitz Syndrome ... Syphilis, Congenital
GENERAL, NEONATAL DISEASES AND DISORDERS
Online Mendelian Inheritance in Man - NCBI (US)
A Gene Map of the Human Genome
, including a list of Featured Genes - NLM/NCBI (US)
Genetic/Rare Conditions, Support Groups and Information
- KUMC (US)
The US National Organization for Rare Disorders , and a list of its Member Organizations
Resources for People with Facial Difference
, 1997 ed. - Lets Face It
About Some Spinal Cord and Brain Development Disorders - Boston Univ. (US)
Association of Birth Defect Children
, Inc. - (US)
Rare Genetic Diseases in Children
- N Y Medical C. (US)
On Genetic Disorders - (US)
The GeneCards Encyclopedia - Weizmann Institute (IL)
GENLINE - Medical Genetics Knowledge Database
Genetic Drift Newsletter and Newborn Screening Practitioner's Manual - MSRGSNet, Arizona (US) Genetic Testing Information from GeneCare, Inc. (US) Fill Out Your Own Family Health History Tree - AMA (US) Developmental Medicine Textbook - Develop. Med. Forum

49. B PARENTS EXCHANGE Genetics /b
Foundation Dandy Walker Syndrome Directory of Genetic Support Groups Table of GeneticDisorders FG Syndrome Hemophilia jacobsen syndrome Klinefelter Syndrome
http://members.tripod.com/~pex/genetics.html
Get Five DVDs for $.49 each. Join now. Tell me when this page is updated
Intro to Genetic Testing

The Achromatopsia Network
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Intro to Genetic Testing

The Achromatopsia Network
...
Return to Disability List

50. PEDIATRICS
Intraventricular Hemorrhage (IVH), Gross Path Specimen Intravenous Immune Globulin(IVIG) Iron Needs of Infants J jacobsen syndrome (11q) Jaundice, Management
http://members.tripod.com/~gustavo_01/pediatri.html

LinkExchange Member

PEDIATRICS
ATENÇO:
Você vai encontrar ainda textos relacionadas com essa especialidade em Medicina de Emergência
ATENTION: See still Topics related with this speciality in Emergency Medicine
A
Acute Respiratory Distress Syndrome

Alpha-1 Antitrypsin Deficiency

Amniocentesis

Amniotic Band Syndrome
...
Audiology Screening Criteria for Neonates
B Baby Walkers, Accident Prevention Biliary Atresia Biliary Atresia BPD Mortality Calculation ... Breastfeeding, Nutrition Requirements C Calcium, Phosphate, and Magnesium Homeostasis Care of the Premature Infant: Part I. Monitoring Growth and Development Cause-Specific Infant Mortality Rate in Qatif Area, Eastern Province, Saudi Arabia Chickenpox (Varicella) ... Cystic Fibrosis D De Lange Syndrome Diaphragmatic Paralysis in the Newborn Discharge after Normal Term Birth Down Syndrome (Trisomy 21) ... Duodenal Atresia E Early Discharge from the NICU Early Discharge Early Discharge of Term Healthy Newborns at Less Than 24 Hours of Age Enteral Feedings for the Premature Infant ... Evaluation and Treatment of Urinary Tract Infections in Children F Feeding of Premature Infants Feeding the Premature Infant Fetal Alcohol Syndrome Fetal Blood Sampling (FBS) ... Fiberoptic, Conventional and Combination Phototherapy for Treatment of Nonhemolytic Hyperbilirubinemia in Neonates

51. Fetal Syndromes
PAGE Gorlin Syndrome Features/OMIM; Images Patient Info Contacta Family; Search Literature. BACK TO TOP OF PAGE jacobsen syndrome
http://www.perinatology.com/ultrasound/syndromes.htm
perinatology.com
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    52. Dr Slijepcevic
    by a new telomere. This chromosome breakage has a specific phenotype,disease known as jacobsen syndrome. We are currently using
    http://www.brunel.ac.uk/depts/bio/staff/slip.htm
    Dr. Predrag Slijepcevic.
    BA , Veterinary Medicine, University of Sarajaevo, 1986
    MSc., Radiation Biology, University of Sarajevo, 1987
    PhD., Radiation Biology, University of Sarajevo, 1991
    Contact details Module Coordinator Also teaches on Room Number - 239
    Tel. Extension - 2109
    EMail - predrag.slijepcevic@brunel.ac.uk BB3091, Final Year Projects
    BB1012 Genetics 1
    BB2011 Genetics 2 Research Activities
    Telomere biology Telomeres are specialised structures at chromosome termini implicated in cellular ageing and carcinogenesis. Our research is focused on understanding the mechanisms of telomere length regulation in mammalian cells, as well as the mechanisms of new telomere acquisition following spontaneous or induced chromosome breakage. We have demonstrated that interstitial telomeric sequences present in chromosomes of many vertebrate species are sensitive to both spontaneous and induced chromosome breakage. A model has been proposed to explain breakage sensitivity of interstitial telomeric sites. In addition, we have demonstrated acquisition of a new telomere at 11q23.3 in the human genome: chromosome breakage occurred within the FRA11B fragile site and broken chromosome was stabilised by a new telomere. This chromosome breakage has a specific phenotype, disease known as Jacobsen syndrome. We are currently using Q-FISH (quantitative fluorescence in situ hybridization) to study telomere length regulation in normal and mutant mammalian cells. These studies revealed that telomere length is chromosome-specific, and that centromere position affects telomere length in individual chromosomes. Telomeres closer to centromeres appear to be shorter than their counterparts more distant from centromeres. A model designed to explain this centromere position effect has recently been proposed and we are currently testing the model. We have also identified a telomere phenotype associated with the murine

    53. Malattie Rare E Genetiche Lettera "J"
    syndrome de••{} * Jakob Creutzfeld Malattia di= Vedi Malattia di CreutzfeldJakob* Jacobsen Sindrome di••jacobsen syndrome de•Jacobsen, Síndrome de
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    54. Links: Health: Rare Disorders- Alabama Council For Developmental Disabilities
    Pigmenti; Isaacs Syndrome; jacobsen syndrome; Joubert Syndrome; KearnsSayre Syndrome; Kernicterus; KlippelFeil Syndrome; Kluver-Bucy
    http://www.acdd.org/Links/conditions/Rare_Disorders.htm
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    • Cherubs - A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. Contact a Family - Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. Fibrous Dysplasia Support Online - For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. Human Growth Foundation - Information about growth-related disorders through education, research, and advocacy. Member driven organization. International Rare Disease Support Network - A community providing more than a 1000 different links to support groups for the people of all nations. Kindler Syndrome - An article and case study of this rare disease. Includes links. National Organization for Rare Disorders, Inc.

    55. Hi-Tech HyperSearch ... Health:Medical
    WEB site Rate This Site 0.00 / 0 Votes The Fragile Web Site provides informationon the chromosome deletion syndrome, jacobsen syndrome (11q syndrome) as
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    56. Open Directory & Pay Per Click Search Engine: Health/Conditions And Diseases/Rar
    LINKS Danny's 11q Information Page A mother shares her story abouthaving a son with jacobsen syndrome. http//hometown.aol.com
    http://www.searchpixie.com/Health/Conditions_and_Diseases/Rare_Disorders/Jacobse
    Need Traffic TrafficGiveAway.com Search the Web Home Toolbar LinkManager bookmark ... Rare Disorders : Jacobsen Syndrome LINKS:
    • Danny's 11q Information Page
      A mother shares her story about having a son with Jacobsen Syndrome.
      http://hometown.aol.com/deidran/danny.html
    • Institute of Child Health
      An article with an explanation of Jacobsen Syndrome.
      http://www.ich.ucl.ac.uk/units/mhu/fws/frames/jsoframe.htm
    • NORD - Jacobsen Syndrome
      A look at the alternate names, a general discussion and resources.
    • The Fragile WEB Site
      Information on Jacobsen syndrome, the chromosome deletion syndrome, for the families and carers of JS patients. Reference databaase, family support groups and clinical information.
      http://web.ukonline.co.uk/c.jones/contents.htm
    HOME ADD A LINK MODIFY A LINK LOGIN ... Affiliate Program

    57. Open Directory & Pay Per Click Search Engine: Health/Conditions And Diseases/Rar
    Cleidocranial Dysplasia (6). Cystinosis (5). Degos (4). Erythromelalgia (4).jacobsen syndrome (4). Melorheostosis (3). Moyamoya (5). Ollier Disease (3).
    http://www.searchpixie.com/Health/Conditions_and_Diseases/Rare_Disorders/
    Need Traffic TrafficGiveAway.com Search the Web Home Toolbar LinkManager bookmark ... Conditions and Diseases : Rare Disorders CATEGORIES: Agnosia Aicardi Syndrome Alstrom Syndrome Barth Syndrome ... Wegener's Granulomatosis LINKS:
    • Cherubs
      A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia.
      http://www.cherubs-cdh.org
    • Contact a Family
      Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK.
      http://www.cafamily.org.uk
    • Fibrous Dysplasia Support Online
      For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism.
      http://members.cox.net/fdsupport/index.html
    • Human Growth Foundation
      Information about growth-related disorders through education, research, and advocacy. Member driven organization. http://www.hgfound.org/
    • International Rare Disease Support Network A community providing more than a 1000 different links to support groups for the people of all nations. http://www.raredisorders.com

    58. Canadian Directory Of Genetic Support Groups
    Chromosome) Trisomy 9 International Parent Support ( Trisomy 9) (Chromosome) 11qResearch and Resource Group (jacobsen syndrome11q- syndrome) Chromosome 11
    http://www.lhsc.on.ca/programs/medgenet/c_sup.htm

    Index by
    support group Canadian Directory of Genetic Support Groups
    Canadian Alopecia Areata Association (Alopecia Areata)
    Canadian Angelman Syndrome Society
    (Angelman Syndrome)
    C.A.S.T. (Canadian Arthrogryposis Support Team)
    (Arthrogryposis)
    Canadian Association for Community Living
    (Down Syndrome, Developmental Delay, Autism, Chromosome Abnormality, Trisomy 18, 13)
    Canadian Association for Williams Syndrome (CAWS)
    (Williams Syndrome)
    Canadian Association for People Who Stutter (CAPS)
    (Stuttering)
    Canadian Association of Friedreich's Ataxia
    Friedreich's Ataxia)
    Canadian Association of Speech-Language Pathologists and Audiologists
    Hearing Impairment, Speech Impairment, Deafness)
    Canadian Cancer Society
    (Cancer) Canadian Celiac Association (Celiac Disease) Canadian Centre on Substance Abuse (Abuse of alcohol, tobacco and other drugs)

    59. Untitled
    Prenatal diagnosis of jacobsen syndrome. jacobsen syndrome is a contiguous genedeletion syndrome caused by the deletion of chromosome 11q23 to qter.
    http://www.faseb.org/genetics/ashg00/f2381.htm

    60. Untitled
    Program Nr 808 jacobsen syndrome four Korean children with thrombocytopeniaor neutropenia. EJ Seo, SM Ahn, JY Lee, HW Yoo. Medical
    http://www.faseb.org/genetics/ashg00/f808.htm

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