Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis

about

Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis

Item

http://www.wikidata.org/entity/Q37224321

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 31 August 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Rare congenital chromosomal aberration dic

@nl

Rare congenital chromosomal ab ...... ent with primary myelofibrosis

@en

type

Item

label

Rare congenital chromosomal aberration dic

@nl

Rare congenital chromosomal ab ...... ent with primary myelofibrosis

@en

prefLabel

Rare congenital chromosomal aberration dic

@nl

Rare congenital chromosomal ab ...... ent with primary myelofibrosis

@en

P1476

Rare congenital chromosomal ab ...... ent with primary myelofibrosis

@en

P2093

Lucie Bartuskova

http://www.w3.org/2001/XMLSchema#string

Martina Langova

http://www.w3.org/2001/XMLSchema#string

Pavlina Malikova

http://www.w3.org/2001/XMLSchema#string

P2860

A compendium of cytogenetic abnormalities in myelofibrosis: molecular and phenotypic correlates in 826 patients.

Skeletal Deformity Associated with SHOX Deficiency

Chromosomal variants in klinefelter syndrome.

Transcriptional regulators of chondrocyte hypertrophy.

Is there an association with constitutional structural chromosomal abnormalities and hematologic neoplastic process? A short review.

Short stature due to SHOX deficiency: genotype, phenotype, and therapy.

Unique karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian patient with Ovotesticular disorder of sexual development.

Klinefelter syndrome and cancer: from childhood to adulthood.

Molecular genetic evaluation of myeloproliferative neoplasms.

45,X/46,X,psu dic(Y) gonadal dysgenesis: influence of the two cell lines on the clinical phenotype, including gonadal histology.

P2888

s13039-016-0276-2

P304

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

case report

P356

10.1186/S13039-016-0276-2

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

P577

2016-08-31T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27588041

http://www.w3.org/2001/XMLSchema#string

P921

birth defect

P932

5007838

http://www.w3.org/2001/XMLSchema#string