ATR-16 due to a de novo complex rearrangement of chromosome 16

Hemoglobin

Volumn 29, Issue 2, 2005, Pages 141-150

  Gallego, Marta S ^a   Zelaya, Gabriela ^a   Feliu, Aurora S ^a   Rossetti, Liliana ^b   Shaffer, Lisa G ^c   Bailey, Kristen A ^d   Bacino, Carlos A ^c   Barreiro, Cristina Z ^a  

^a HOSPITAL DE PEDIATRÍA PROF DR JUAN P GARRAHAN   (Argentina)

^b INSTITUTO DE INVESTIGACIONES EN INGENIERÍA GENÉTICA Y BIOLOGÍA MOLECULAR   (Argentina)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

ATR 16; Duplication 16q; Subtelomeric probe

Indexed keywords

ALPHA GLOBIN;

ADULT; ALPHA THALASSEMIA; ANEMIA; ARTICLE; BLOOD ANALYSIS; CASE REPORT; CELL INCLUSION; CHROMOSOME 16Q; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; DNA DETERMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HUMAN; INFANT; IRON DEFICIENCY ANEMIA; MALE; MARKER GENE; MENTAL DEFICIENCY; MICROSATELLITE MARKER; MOTHER CHILD RELATION; NUCLEOTIDE SEQUENCE; TELOMERE;

ALPHA-THALASSEMIA; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 16; CYTOGENETIC ANALYSIS; DNA MUTATIONAL ANALYSIS; GENOTYPE; HEMOGLOBIN H; HEMOGLOBINS, ABNORMAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MENTAL RETARDATION; POINT MUTATION; SEQUENCE DELETION;

EID: 18844365139     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-200058585     Document Type: Article

References (21)

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