A syndrome involving intrauterine growth retardation, microcephaly, cerebellar hypoplasia, B lymphocyte deficiency, and progressive pancytopenia.

Pediatrics

Volumn 105, Issue 3, 2000, Pages

  Revy, P ^a   Busslinger, M ^a   Tashiro, K ^a   Arenzana, F ^a   Pillet, P ^a   Fischer, A ^a   Durandy, A ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA CHEMOKINE; CHEMOKINE RECEPTOR CXCR4; DNA BINDING PROTEIN; PAX5 PROTEIN, HUMAN; PROTEIN; STROMAL CELL DERIVED FACTOR 1; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PAX5;

AGAMMAGLOBULINEMIA; ARTICLE; B LYMPHOCYTE; BLOOD; CASE REPORT; CELL DIFFERENTIATION; CEREBELLUM; CONGENITAL MALFORMATION; CYTOLOGY; FEMALE; GENETICS; HUMAN; INTRAUTERINE GROWTH RETARDATION; MICROCEPHALY; NEWBORN; PANCYTOPENIA; SYNDROME;

AGAMMAGLOBULINEMIA; B-CELL-SPECIFIC ACTIVATOR PROTEIN; B-LYMPHOCYTES; CELL DIFFERENTIATION; CEREBELLUM; CHEMOKINES, CXC; DNA-BINDING PROTEINS; FEMALE; FETAL GROWTH RETARDATION; HUMANS; INFANT, NEWBORN; MICROCEPHALY; PANCYTOPENIA; PROTEINS; RECEPTORS, CXCR4; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0034145866     PISSN: None     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.105.3.e39     Document Type: Article

References (0)