41. FANCC - Fanconi Anemia, Complementation Group C - Aka: FAC, FACC - Cancer Geneti FANCC; fanconi anemia, complementation group C. Human alpha Spectrin II and thefanconi anemia Proteins FANCA and FANCC Interact to Form a Nuclear Complex. http://www.cancerindex.org/geneweb/FANCC.htm

Cancer Genetics Web www.cancer genetics.org FANCC ; Fanconi anemia, complementation group C (9q22.3) FANCC Menu Summary Information - FANCC Gene Database Entries for FANCC Other FANCC Related Resources FANCC - Fanconi Anaemia Complementation Group C ... Feedback / suggest a new topic for FANCC Search: Summary Information FANCC; Fanconi anemia, complementation group C Location: Aliases: FAC, FACC Return to FANCC Contents Gene Database Entries for FANCC OMIM GeneCard (Weizmann Institute) Atlas of Genetics and Cytogenetics in Oncology and Haematology Human Gene Mutation Database (Cardiff, UK) Genbank Locus Link UniGene GenAtlas ... Nomenclature (search for FANCC) Return to FANCC Contents Other Related Resources Fanconi Anaemia Resources Medline Search: (FACC OR FAC OR FANCC) AND FANCONI ANAEMIA (PubMed) Limit search to: [Last Year] Limit search to: [Last 2 Years] Limit search to: [Reviews] Medline Search: FACC OR FAC OR FANCC (PubMed) Limit search to: [Last Year] Limit search to: [Last 2 Years] Limit search to: [Reviews] Search Medline for related articles (PubMed) Medline Search: cancer AND gene AND (FANCC[TI] OR FAC[TI] OR FACC[TI]) (PubMed) Limit search to: [Last Year] Limit search to: [Last 2 Years] Limit search to: [Reviews] Return to FANCC Contents FANCC - Fanconi Anaemia Complementation Group C McMahon LW, et al.

42. Fanconi Anemia Z . Back Home Next. fanconi anemia. fanconi anemia A Handbook forFamilies Their Physicians. fanconi anemia Research Fund. Fanconi http://www.ability.org.uk/Fanconi_Anemia.html

Our Aims Services Stats ... Z Fanconi Anemia Fanconi Anemia Research Fund Fanconi Anaemia - A rare disorder found in children that involves the blood and bone marrow. Genetically Transmitted Ailments - Information Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

43. Fanconi Anemia fanconi anemia fanconi anemia A Handbook for Families Their Physicians Givesbasic information, in plain language, about understanding and coping with a http://www.ability.org.uk/Facial_Differences.html

Our Aims Services Stats ... Z Fanconi Anemia - Gives basic information, in plain language, about understanding and coping with a serious disorder known as Fanconi anemia, or Fanconi's anemia. Fanconi Anemia Research Fund Fanconi Anaemia - A rare disorder found in children that involves the blood and bone marrow. Siniawski, Jake - For Jake's Sake. Jake's life with Fanconi Anemia. Genetically Transmitted Ailments - Information Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

44. MedWebPlus Subject Diseases And Conditions Hereditary Diseases A, , GO, fanconi anemia a Handbook for Families Their Physicians 2nd ed.,1995 / Lynn and Dave Frohnmayer. A, -, GO, Leukaemia Research Fund Fanconi Anaemia. http://www.medwebplus.com/subject/Diseases_and_Conditions/Hereditary_Diseases/Fa

Main About MWP Contribute to MWP Contact Us A service of Flexis, Inc. Welcome to MedWebPlus 2.3! A free service to help you find health sciences information quickly and easily. Diseases and Conditions Hereditary Diseases Fanconi's Anemia Web Sites: A GO Fanconi Anemia Research Fund A GO 2nd ed., 1995 / Lynn and Dave Frohnmayer A GO Leukaemia Research Fund Fanconi Anaemia A GO Online Mendelian Inheritance in Man FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA A GO Online Mendelian Inheritance in Man FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC A GO Online Mendelian Inheritance in Man FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD Flexis, Inc. Privacy statement Powered by y-Base

45. MedWebPlus Web Site ID 10913 Online Mendelian Inheritance in Man fanconi anemia, COMPLEMENTATION GROUP A;FANCA (227650). http//www3.ncbi.nlm.nih.gov/htbinpost/Omim/dispmim?227650 http://www.medwebplus.com/obj/10913

Main About MWP Contribute to MWP Contact Us A service of Flexis, Inc. Welcome to MedWebPlus 2.3! A free service to help you find health sciences information quickly and easily. Online Mendelian Inheritance in Man FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA (227650) http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?227650 Uptime grade: A Usage grade: Popularity: N/A Location: North America United States Maryland Bethesda Subjects: All Diseases Diseases and Conditions Genetics Hematology ... Privacy statement Powered by y-Base

46. GeneReviews: Fanconi Anemia Your browser does not support HTML frames so you must view fanconi anemiain a slightly less readable form. Please follow this link to do so. http://www.geneclinics.org/profiles/fa&id=8888888&key=vLsPZfF5ieW3O

Your browser does not support HTML frames so you must view Fanconi Anemia in a slightly less readable form. Please follow this link to do so.

47. Fanconi Anemia Research Studies There are 7 complementationgroup subtypes (A, B, C, D1, D2, E, F, G) for fanconi anemia.......fanconi anemia Research Studies. Subtyping http://research.dfci.harvard.edu/dandrealab/faresearch.html

Fanconi Anemia Research Studies Subtyping Mutational Analysis Amifostine Tumor Studies ... Development of New Clinical Tests for the Diagnosis and Management of Fanconi Anemia Subtyping: Description: Our laboratory is performing subtyping analysis on a research basis. A small sample of blood (about one teaspoon) obtained at a time when blood is being drawn for clinical reasons can be used for these studies. The blood cells (lymphocytes) are immortalized with a virus (Epstein Barr virus or EBV, which is the virus that causes mononucleosis) and grown in culture for testing. The patient's subtype is identified by testing the ability of an introduced Fanconi gene (A, C, D2, E, F, or G) to correct the cell's sensitivity to DNA damaging agents such as mitomycin C (MMC) or diepoxybutane (DEB). Fanconi cells cannot repair the DNA damage inflicted by these agents. Introduction of the functional homologue of the defective Fanconi gene can restore the cellsâ ability to repair its DNA. The cells are then frozen and stored for additional studies. A family can choose to withdraw from these studies at any time. These tests take several weeks to complete. Sometimes, cells from Fanconi patients do not grow well in culture. We would let you know if this were the case, and you would have the option of submitting another sample for testing.

48. Comprehensive Center For Fanconi Anemia A fanconi anemia and Chromosome Instability Center has been established atDanaFarber Cancer Institute and Children's Hospital in Boston. http://research.dfci.harvard.edu/dandrealab/fanconianemia.html

Comprehensive Center For Fanconi Anemia Dana Farber Cancer Institute A Fanconi Anemia and Chromosome Instability Center has been established at Dana-Farber Cancer Institute and Children's Hospital in Boston. The center is directed by Dr. Alan D'Andrea, M.D., Professor of Pediatrics. This Center offers a wide range of services including: o A basic research program in the molecular and cellular biology of Fanconi Anemia, conducted in the laboratory of Dr. D'Andrea. o The creation of a Fanconi Anemia patient cell repository, including lymphoblastoid cell lines, skin fibroblast cell lines, and tumor cell lines from patients and family members. This repository has been assembled in collaboration with Dr. Markus Grompe and the Oregon Health Sciences University (OHSU). o A Registry of FA patients from across the United States and Canada, including clinical information and family history. o A Cytogenetics Core Laboratory at the Dana-Farber (Mayer Bldg., room 676) (headed by Lisa Moreau ) for diagnosis, DEB testing, complementation group analysis, and carrier detection. o A diagnostic and evaluation center for new and known patients with Fanconi Anemia, which is directed by

49. Fanconi Anemia Research Fund, Inc. fanconi anemia Research Fund, Inc. International network. Provides support and exchangeof information regarding medical advances in fanconi anemia research. http://www.medhelp.org/amshc/amshc254.htm

Title: Aplastic Anemia and MDS International Foundation, Inc. Description: Emotional support for persons with aplastic anemia, myelodysplastic syndromes and other bone marrow failure diseases. Financially supports research. Provides free educational materials and updated medical information. Scope: International Number Groups: 25 chapters Founded: Address: P.O. Box 613 Annapolis, Maryland, 21404 United States Telephone: 1-800-747-2820 or (410)867-0242 Fax: Email: help@aamds.org Web Address: http://www.aamds.org This information has been generously provided by The American Self Help Clearinghouse and hosted by Med Help International . Please send corrections/updates to ed@selfhelpgroups.org Updated: 02/2003

50. JAMA -- Page Not Found Preimplantation Diagnosis for fanconi anemia Combined With HLA Matching Author InformationYury Verlinsky, PhD; Svetlana Rechitsky, PhD; William Schoolcraft, MD http://jama.ama-assn.org/issues/v285n24/abs/jbr00301.html

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery MSJAMA Science News Updates Meetings Peer Review Congress The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"

51. Health Information Resource Database: Fanconi Anemia Research Fund, Inc. fanconi anemia Research Fund, Inc. Contact Information. Abstract. fanconi anemiaResearch Fund, Inc., is a nonprofit corporation established in 1989. http://www.health.gov/nhic/NHICScripts/Entry.cfm?HRCode=HR2438

52. Genzyme Corporation - Genetics fanconi anemia (FA) is an inherited anemia that leads to bone marrow failure (pancytopenia).There is considerable variability in age and mode of presentation. http://www.genzymegenetics.com/genetics/clinicalinfo/molgen/fanconi.htm

53. Fanconi Anemia (Type C), DNA Analysis (511212) fanconi anemia (Type C), DNA Analysis (511212). Auerbach AD, fanconi anemiaGenetic Testing in Ashkenazi Jews, Genet Test, 1997, 1(1)2733 (review). http://www.labcorp.com/datasets/labcorp/html/chapter/mono/mg003300.htm

Fanconi Anemia (Type C), DNA Analysis (511212) CPT Related Information Chromosome Analysis, Instability Syndromes Jewish Heritage Profile II Synonyms Jewish Heritage, IVS+4 A-T Mutation Specimen Whole blood Volume 7 mL Minimum Volume 3 mL Container Lavender-stopper (EDTA) tube Storage Instructions Maintain specimen at room temperature. Causes for Rejection Frozen specimen; hemolysis; quantity not sufficient for analysis Use Identification of carrier and affected individuals for one mutation associated with Fanconi anemia, type C Limitations This test detects ~99% of the mutations responsible for Fanconi anemia, type C in Ashkenazi Jews. This test is not appropriate for non-Ashkenazi Jewish individuals. Methodology Allele-specific polymerase chain reaction (PCR) and gel electrophoresis References Auerbach AD, "Fanconi Anemia: Genetic Testing in Ashkenazi Jews," Genet Test , 1997, 1(1):27-33 (review).

54. Fanconi Anemia (Type C) And Niemann-Pick Disease, DNA Analysis ( fanconi anemia (Type C) and NiemannPick Disease, DNA Analysis (512129).CPT 83890; 83893 (x4); 83894 (x2); 83896 (x8); 83898 (x2 http://www.labcorp.com/datasets/labcorp/html/chapter/mono/mg003600.htm

Fanconi Anemia (Type C) and Niemann-Pick Disease, DNA Analysis (512129) CPT Related Information Chromosome Analysis, Instability Syndromes Synonyms Acid Sphingomyelinase Gene; Jewish Heritage, IVS+4 A-T Mutation Test Includes Fanconi anemia (type C), DNA analysis; Neimann-Pick disease (type C), DNA analysis Specimen Whole blood Volume 7 mL Minimum Volume 3 mL Container Lavender-stopper (EDTA) tube Storage Instructions Maintain specimen at room temperature. Causes for Rejection Frozen specimen; hemolysis; quantity not sufficient for analysis Use Identification of carrier and affected individuals for one mutation associated with Fanconi anemia C and identification of carrier and affected individuals for four mutations associated with Neimann-Pick disease, types A and B Limitations This test detects ~95% of the mutations responsible for Niemann-Pick disease, types A and B in Ashkenazi Jews and detects ~99% of the mutations responsible for Fanconi anemia, type C in Ashkenazi Jews. This test is not appropriate for non-Ashkenazi Jewish individuals. Methodology Polymerase chain reaction (PCR) and allele-specific oligonucleotide (ASO) analysis and allele-specific polymerase chain reaction (PCR) and gel electrophoresis References Auerbach AD, "Fanconi Anemia: Genetic Testing in Ashkenazi Jews,"

55. BloodMed - General Section Go to top. Fanconi's anemia (Argentina). Asociation Civil Argentina de Anemiade Fanconi. Fanconi's anemia Canada. Canadian fanconi anemia Research Fund. http://www.bloodmed.com/home/patient.asp

The global source for hematology education, practice and research Privacy statement ISSN: 1478-1247 Aplastic anemia Cancer - child Diamond Blackfan anemia Eosinophilia-myalgia syndrome ... Sickle cell anemia - West Indies 6 If you wish to add your organization to the list please Aplastic anemia The Aplastic Anaemia Trust Cancer - child Childhood Leukemia Foundation Diamond Blackfan anemia DBA Foundation Eosinophilia-myalgia syndrome National Eosinophilia-Myalgia Syndrome Network Fanconi's anemia (Argentina) Asociation Civil Argentina de Anemia de Fanconi Cesar and Irma de Leon Fanconi's anemia - Canada Canadian Fanconi Anemia Research Fund Tami and Peter Dunstan-Adams Fanconi's anemia - France Association relative a la maladie de Fanconi Fanconi's anemia - Germany German Fanconi Anemia Association Ralf Dietrich Fanconi's anemia - India India Family Support Group Fanconi's anemia - Italy AIRFA (Associazione Italiana per la Ricerca sull' Anemia di Fanconi) Via Francesco Saverio Correra Fanconi's anemia - Mexico Asociation Anemia Fanconi Rocio Gomez Gutierrez Fanconi's anemia - The Netherlands Nederlandse Stichting Fanconi Anaemie Ron and Monique Baas Fanconi's anemia - South Africa South African Family Support Group Charles and Dawn Church Gaucher disease National Gaucher Foundation Hemochromatosis American Haemochromatosis Society Iron Disorders Institute Inc.

56. Cameron Goodrich's Support Site fanconi anemia (FA) is named for a Swiss pediatrician, Guido Fanconi.In 1927 Dr. Fanconi published his clinical observations on http://www.totalmayhem.net/cameron/whatisfanconi.htm

Fanconi Anemia (FA) is named for a Swiss pediatrician, Guido Fanconi. In 1927 Dr. Fanconi published his clinical observations on brothers who had inherited various abnormal physical conditions, and also experienced bone marrow failure. These children suffered severe life-threatening aplastic anemia. Their blood systems could not successfully combat infection, fatigue, spontaneous hemorrhage, or bleeding. Recent research shows these discoveries: FA is one of several deadly inherited anemias Both parents must be carriers of a recessive FA gene for their child to be born with this disorder. If both parents carry the recessive gene the chances are one in four that any of their children will inherit the disease. FA patients may have a variety of noticeable birth defects, ranging from minor to serious. These defects may affect every major system of the body. Other FA patients are free from any visible disorderother than the ultimate bone marrow failure. FA patients experience a high incidence of leukemia (10%-15%).

57. Fanconi Anemia - Cameron Goodrich's Memorial Site Always You're Our Hero! Home What is fanconi anemia? Cameron'sBattle Pictures Cameron Desperately Needs Your Help! This http://www.totalmayhem.net/cameron/

We Love You Cameron and Will Miss You Always... You're Our Hero! Home What is Fanconi Anemia? Cameron's Battle Pictures ... Cameron Desperately Needs Your Help! This site best viewed with IE 5+ at 800 x 600 resolution FastCounter by bCentral .: admin only :.

58. The Doctor's Lounge: Fanconi Anemia Review! fanconi anemia. Hematology. Medical disease review for USMLE, MRCP. Hematology.fanconi anemia. Autosomal Recessive congenital pancytopenia. http://www.thedoctorslounge.net/clinlounge/diseases/hematology/fanconi.htm

Home Member Search Discussion ... Contact With over 1 million users and awarded Yahoo site of the day! Start page Favorites TRANSLATE... Italian English Portugese French Spanish German Get FREE Medical Consultation! Meet the Lounge Doctors! Join the Mailing List Ask a doctor ... Membership Student Student Lounge Medical Tutorials Medical Games Discussion ... Membership Professional Discussion Specialty Medline search Guidelines search ... Membership Send TheDoctorsLounge a BIG Thank You! Back to hematological diseases index Hematology Fanconi anemia Autosomal Recessive congenital pancytopenia. Patients with Fanconi's Anemia rarely live beyond their teens or early twenties. Clinical suspicion Fanconi anemia may occur in any nationality and ethnic group, but one particular gene change is responsible for approximately 83% of cases of Fanconi anemia in Jews of Eastern European descent (Ashkenazi Jews). This allows Ashkenazi Jews to be easily tested for Fanconi anemia. Approximately one in 89 Ashkenazi Jews is a carrier of Fanconi anemia. Fanconi Anemia usually reveals itself when children are between the ages of 3-12 years present with extreme fatigue, and frequent infections or recurrent nosebleeds and bruising.

59. Fanconi Anemia fanconi anemia up. Fanconi's anaemia, One in a series of brief leafletsabout leukaemia and related diseases directed at the public. http://omni.ac.uk/browse/mesh/detail/C0015625L0015625.html

Fanconi Anemia [up] Fanconi's anaemia One in a series of brief leaflets about leukaemia and related diseases directed at the public. The document provides key information such as the causes, signs and symptoms, diagnosis, treatment, and prognosis of fanconi anaemia (an inherited form of aplastic anaemia in which the bone marrow fails to produce blood cells normally). Published on the web by the Leukaemia Research Fund. Fanconi Anemia Patient Education Handout [Publication Type] Last modified 28/Mar/2003 [Low Graphics]

60. FANCONI ANEMIA Post Followup Return to Message Listings Print Message fanconi anemia Postedby Gayle (ID *****5165) Date February 02, 2003 at 172031 of 34264. http://genforum.genealogy.com/italy/messages/34155.html

Chat Daily Search My GenForum Community Standards ... Terms of Service Jump to Forum Home Regional Countries Italy Genealogy Forum FANCONI ANEMIA Posted by: Gayle (ID *****5165) Date: February 02, 2003 at 17:20:31 of 35565 Fanconi Aplastic Anemia-a lethal genetic blood/bone marrow disease- it is a non-discriminating genetic disease. The only treatment is a bone marrow transplant. Each parent must be a carrier of the gene in order to pass the gene on to his or her child. Known Italian families this illness has presented itself. Di Lullo, Napoles, Quilici, Russo, Di Mercurio, Apollo, De Persis, Archiello, Della Ratta, Di Marino, Fiaschetti, Senatore, De Bonis, Ceresa, Briga, De Marco, Ciccolini, Frontani, Mignone, Pagano People interested in helping may become bone marrow donors to help save a child’s life. Identical matches are found in ones ethnic family. Support ongoing research through the Fanconi Anemia Research Fund , INC 1801 Willamette Street, Suite 200 Eugene, Oregon 97401 or www.fanconi.org. They support research around the world including research centers in Naples and Milan, Italy. Mille grazie, Gayle L.

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