Incidental detection of Chiari malformation in Fanconi anaemia

British Journal of Haematology

Volumn 158, Issue 2, 2012, Pages 154-

  Deepak Amalnath, S ^a   Subramanian, Rama ^a   Swaminathan, R P ^a   Indumathi, N ^b  

^a JAWAHARLAL INSTITUTE OF POSTGRADUATE MEDICAL EDUCATION AND RESEARCH   (India)

^b APOLLO HOSPITALS   (India)

Author keywords

[No Author keywords available]

Indexed keywords

MITOMYCIN C;

ADULT; ANEMIA; ARNOLD CHIARI MALFORMATION; BONE MARROW DEPRESSION; BRAIN HERNIA; CAFE AU LAIT SPOT; CASE REPORT; CHROMOSOME BREAKAGE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DISEASE ASSOCIATION; DISEASE DURATION; FANCB GENE; FANCONI ANEMIA; GENE; GENE MUTATION; GENETIC RISK; HEADACHE; HUMAN; HYDROCEPHALUS; LIMB MALFORMATION; MALE; NEUROLOGIC EXAMINATION; NOTE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCREENING TEST; SYRINGOMYELIA; THUMB MALFORMATION; X CHROMOSOME LINKAGE;

ARNOLD-CHIARI MALFORMATION; BRAIN; FANCONI ANEMIA; HUMANS; INCIDENTAL FINDINGS; MAGNETIC RESONANCE IMAGING; MALE; YOUNG ADULT;

EID: 84863445282     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2012.09195.x     Document Type: Note

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