Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations.

about

Molecular Subgroups of Glioblastoma- an Assessment by Immunohistochemical Markers.Clinical feature of infertile men carrying balanced translocations involving chromosome 10: Case series and a review of the literature.

P2860

Q47929342-F2CBB98E-436F-407E-971D-AD9EB552B7A3 Q52593821-11407F50-41BE-4ABA-949D-FB8DC8A8AD54

P2860

Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations.

Item

http://www.wikidata.org/entity/Q36815458

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Clinical and molecular cytogen ...... ith imbalanced translocations.

@ast

Clinical and molecular cytogen ...... ith imbalanced translocations.

@en

type

Item

label

Clinical and molecular cytogen ...... ith imbalanced translocations.

@ast

Clinical and molecular cytogen ...... ith imbalanced translocations.

@en

prefLabel

Clinical and molecular cytogen ...... ith imbalanced translocations.

@ast

Clinical and molecular cytogen ...... ith imbalanced translocations.

@en

P1476

Clinical and molecular cytogen ...... ith imbalanced translocations.

@en

P2093

Dong Wu

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

Fei Fei Huang

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

Hong Dan Wang

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

Hong Yan Liu

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

Jia Huang

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

Liang Jie Guo

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

Qian Nan Guo

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

Rui Li Wang

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

Tao Li

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

Tao Wang

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

P2860

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)

Absence of ghrelin protects against early-onset obesity

Phelan-McDermid Syndrome and SHANK3: Implications for Treatment.

Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities.

Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.

Chromosomal Translocation t (10;19) (q11.2;q13.4) in an Infertile Male

Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.

Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4.

Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)

P2888

s13039-016-0244-x

P304

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

P31

scholarly article

P356

10.1186/S13039-016-0244-X

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

P478

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

P577

2016-04-19T00:00:00Z

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

P6179

1004671675

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

P698

27099631

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

P932

4837590

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

Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations.

about

P2860

P2860

Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P6179

P698

P932