Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

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Pseudohypoparathyroidism type 1B in a patient conceived by in vitro fertilization: another imprinting disorder reported with assisted reproductive technology.

P2860

Q50126262-52C0E862-0D31-4792-A36C-C60E63C82026

P2860

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

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http://www.wikidata.org/entity/Q50119101

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

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2017年學術文章

@zh-hant

name

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

@en

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

@nl

type

Item

label

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

@en

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

@nl

prefLabel

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

@en

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

@nl

P1476

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology

@en

P2093

Harald Jüppner

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Joel Riquelme

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Maria Jose Zambrano

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Marie-Laure Kottler

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

Monica Fernandez

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

Veronica Mericq

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P2860

Pseudo-pseudohypoparathyroidism

Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism: possible cerebral imprinting of Gsalpha

Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism.

Genetic imprinting during impaired spermatogenesis.

A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously.

Familial pseudohypoparathyroidism without somatic anomalies.

Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples.

The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3.

Pseudohypoparathyroidism: assays of parathyroid hormone and thyrocalcitonin.

An update on the clinical and molecular characteristics of pseudohypoparathyroidism.

P304

1125-1132

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scholarly article

P356

10.1515/JPEM-2017-0226

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P433

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

P478

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Claudia Castiglioni

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2017-10-01T00:00:00Z

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28902630

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P932

5938740

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Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

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P2860

P2860

Pseudohypoparathyroidism type 1B associated with assisted reproductive technology.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932