X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26. - Wikidata - awgldk - TriplyDB

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

http://www.wikidata.org/entity/Q35238594

about

Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26 Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3 Genetic regulation of pituitary gland development in human and mouse Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27 Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3.Mir505-3p regulates axonal development via inhibiting the autophagy pathway by targeting Atg12.

P2860

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P2860

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

http://www.wikidata.org/entity/Q35238594

description

1997 nî lūn-bûn

@nan

1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

1997年の論文

@ja

1997年論文

@yue

1997年論文

@zh-hant

1997年論文

@zh-hk

1997年論文

@zh-mo

1997年論文

@zh-tw

1997年论文

@wuu

name

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@ast

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@en

type

label

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@ast

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@en

prefLabel

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@ast

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@en

P1433

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P1476

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P2093

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P2860

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P31

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P433

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P478

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P577

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P698

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P932

Q35238594-4D3F4D5D-1D03-41CE-9C28-F75CFA9786ED

P1433

American Journal of Human Genetics

P1476

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

@en

P2093

Forrest SM

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

Johnsen E

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Lagerström-Fermér M

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Landegren U

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Pettersson U

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Ravine D

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Rickards A

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Sundvall M

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Warne GL

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Zajac JD

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P2860

Detection of specific sequences among DNA fragments separated by gel electrophoresis

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene

Integration of gene maps: chromosome X

A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia

Pit-1-dependent expression of the receptor for growth hormone releasing factor mediates pituitary cell growth

The GDB human genome data base anno 1993

Faster sequential genetic linkage computations

Five polymorphic microsatellite VNTRs on the human X chromosome.

Trinucleotide repeat polymorphism in the androgen receptor gene (AR).

P304

910-916

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P31

scholarly article

P407

P433

4

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P478

60

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P577

1997-04-01T00:00:00Z

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

P698

9106538

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P932

1712462

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