Identity of the abnormal F-group chromosome associated with polycythaemia vera

Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study.

British journal of haematology·1998

Deletions of chromosome 21 restricted to the leukemic cells of children with Down syndrome and leukemia.

Leukemia·1997

Haematological abnormalities in Shwachman-Diamond syndrome.

British journal of haematology·1996

Kostmann's disease, recombinant HuG-CSF, monosomy 7 and MDS/AML.

British journal of haematology·1995

Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system.

Blood·1995

A case of acute megakaryoblastic leukaemia with t(X;6)(p11.21;q23) having an X chromosome breakpoint within a 450-Kb region which is also disrupted in two classes of solid tumours.

Leukemia·1995

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Standard versus miniaturized percutaneous nephrolithotomy in pediatric patients: a systematic review and meta-analysis.

Sao Paulo medical journal = Revista paulista de medicina·2026

Proteinuria as an Unusual Presentation of Pheochromocytoma in Pediatric Patient With Single Kidney.

Case reports in pediatrics·2026

Case Report: Clinical response to TKI therapy in T-cell acute lymphoblastic leukemia with rare ABL1 rearrangement.

Frontiers in oncology·2026

Kaposiform haemangioendothelioma presentation in hand in a paediatric patient.

BMJ case reports·2026

A non-O1/O139 Vibrio cholerae breast abscess in a previously healthy teenager: A case report.

Diagnostic microbiology and infectious disease·2026

Correction to "Tolvaptan: a possible preemptive treatment option in children with autosomal dominant polycystic kidney disease?"

Childhood kidney diseases·2026

Related Experiment Videos

Identity of the abnormal F-group chromosome associated with polycythaemia vera

Related Concept Videos

Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study.

Deletions of chromosome 21 restricted to the leukemic cells of children with Down syndrome and leukemia.

Haematological abnormalities in Shwachman-Diamond syndrome.

Kostmann's disease, recombinant HuG-CSF, monosomy 7 and MDS/AML.

Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system.

A case of acute megakaryoblastic leukaemia with t(X;6)(p11.21;q23) having an X chromosome breakpoint within a 450-Kb region which is also disrupted in two classes of solid tumours.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Standard versus miniaturized percutaneous nephrolithotomy in pediatric patients: a systematic review and meta-analysis.

Proteinuria as an Unusual Presentation of Pheochromocytoma in Pediatric Patient With Single Kidney.

Case Report: Clinical response to TKI therapy in T-cell acute lymphoblastic leukemia with rare ABL1 rearrangement.

Kaposiform haemangioendothelioma presentation in hand in a paediatric patient.

A non-O1/O139 Vibrio cholerae breast abscess in a previously healthy teenager: A case report.

Correction to "Tolvaptan: a possible preemptive treatment option in children with autosomal dominant polycystic kidney disease?"

Related Experiment Videos

Identity of the abnormal F-group chromosome associated with polycythaemia vera

Related Concept Videos

Related Articles