The 17p-syndrome: A distinct myelodysplastic syndrome entity?

Leukemia and Lymphoma

Volumn 25, Issue 1-2, 1997, Pages 163-168

  Jary, L ^a   Mossafa, H ^b,d   Fourcade, C ^a   Genet, P ^c   Pulik, M ^c   Flandrin, G ^d  

^a CENTRE HOSPITALIER VICTOR DUPOUY   (France)

^b LABORATOIRE CERBA   (France)

^c Hopital Necker   (United States)

^d Dept de Genetique Humaine   (France)

Author keywords

17p myelodysplastic syndrome (MDS) peudo Pelger Huet

Indexed keywords

ADULT; AGED; ARTICLE; BLOOD CELL; BONE MARROW BIOPSY; CASE REPORT; CHROMOSOME 17P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 17; DYSGRANULOPOIESIS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

EID: 0031001576     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.3109/10428199709042506     Document Type: Article

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