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IMMUNO-ANALYSE & BIOLOGIE SPECIALISEE, ISSN 0923-2532, 02/2012, Volume 27, Issue 1, pp. 7 - 19
Isochromosome of the long arm of chromosome 20 with interstitial loss of material [ider(20q)] is a rare cytogenetic abnormality reported in myelodysplastic... 
MYELOPROLIFERATIVE DISORDERS | ider(20q) | CHROMOSOME 20Q | DELETED 20Q | ACUTE MYELOID-LEUKEMIA | ISODERIVATIVE CHROMOSOME-20 | Survival | Myelodysplastic syndrome | LONG ARM | del(20q) | ABNORMALITY | Morphology | MALIGNANCIES | PROGNOSTIC-SIGNIFICANCE | MEDICAL LABORATORY TECHNOLOGY | CHRONIC MYELOMONOCYTIC LEUKEMIA
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 02/2007, Volume 27, Issue 2, pp. 143 - 145
Prenatally diagnosed mosaicism for isochromosome 20q is generally reported in association with a normal outcome at birth and is rarely confirmed postnatally.... 
Mosaicism | Trisomy | Isochromosome | AMNIOCENTESIS | mosaicism | GENETICS & HEREDITY | isochromosome | trisomy | CHROMOSOME-20 | OBSTETRICS & GYNECOLOGY | Amniocentesis | Prognosis | Follow-Up Studies | Cell Count | Humans | Child, Preschool | Male | Isochromosomes - genetics | Pregnancy | Adult | Female | Chromosomes, Human, Pair 20 | Infant, Newborn | Pregnancy Outcome | Index Medicus
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 06/2001, Volume 85, Issue 6, pp. 754 - 759
  1 Subsequently, other researchers placed a locus for autosomal dominant CHED (designated CHED1 by the human genome mapping workshop) in an overlapping... 
OPHTHALMOLOGY | HEREDITARY ENDOTHELIAL DYSTROPHY | LINKAGE | CHROMOSOME-20 | Genomes | Chromosomes | Genes | Endothelium | Letters to the Editor
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 03/2004, Volume 75, Issue 3, pp. 488 - 490
Journal Article
MEDICAL SCIENCE MONITOR, ISSN 1234-1010, 03/2005, Volume 11, Issue 3, pp. CS9 - CS15
Background: The influence of the marker chromosome on reproductive failure is difficult to assess, especially in the case of low-rate mosaicism. The aim of our... 
MEDICINE, RESEARCH & EXPERIMENTAL | sperm chromosomes | STRUCTURALLY ABNORMAL CHROMOSOMES | CLINICAL FINDINGS | SUPERNUMERARY RING CHROMOSOME-20 | mosaicism | FISH | IN-SITU HYBRIDIZATION | UNIPARENTAL DISOMY | CAT EYE SYNDROME | INSITU HYBRIDIZATION | PRENATAL-DIAGNOSIS
Journal Article
JOURNAL OF CLINICAL INVESTIGATION, ISSN 0021-9738, 09/1997, Volume 100, Issue 6, pp. 1400 - 1405
Journal Article
AMERICAN JOURNAL OF HUMAN GENETICS, ISSN 0002-9297, 08/1994, Volume 55, Issue 2, pp. 238 - 243
Alagille syndrome is a clinically defined, dominantly inherited disorder affecting the liver, heart, face, eye, and vertebrae. Alagille syndrome has previously... 
LINKAGE MAP | 20P | GENE | ARTERIOHEPATIC DYSPLASIA | GENETICS & HEREDITY | MARKERS | NEUROFIBROMATOSIS | CHROMOSOME-20 | ARM | DELETION
Journal Article
Epileptic Disorders, ISSN 1294-9361, 04/2006, Volume 8, Issue 1, pp. S23 - S32
The identification of an etiology in children and adults with mental deficiency is a major challenge and needs a comprehensive clinical approach and... 
Angelman syndrome | Wolf-Hirschorn | Ring chromosome 20 | Genetic syndromes and epilepsy | AUTISM | ABNORMALITIES | EEG | ANGELMAN-SYNDROME | UBE3A | CLINICAL NEUROLOGY | CHILDREN | ring chromosome 20 | FRAGILE-X-SYNDROME | genetic syndromes and epilepsy | DUPLICATION | RING CHROMOSOME-20 | GENERALIZED EPILEPSY
Journal Article
Progress in Natural Science, ISSN 1002-0071, 08/2005, Volume 15, Issue 8, pp. 757 - 760
Benign familial neonatal convulsions (BFNC) is a rare autosomal dominant inherited epilepsy syndrome. Two voltage-gated potassium channel genes, KCNQ2 and... 
Mutation analysis | Potassium channel | BFNC | Epilepsy | Linkage analysis | epilepsy | linkage analysis | mutation analysis | MULTIDISCIPLINARY SCIENCES | KCNQ2 | MUTATION | potassium channel | POTASSIUM CHANNEL GENE | CHROMOSOME-20
Journal Article
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