(Q34032271)

30 July 2017

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title

Genetic control of intra-uterine growth (English)

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30 July 2017

Devriendt K

1

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30 July 2017

publication date

1 September 2000

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European Journal of Obstetrics Gynecology and Reproductive Biology

30 July 2017

published in

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30 July 2017

volume

92

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30 July 2017

issue

1

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30 July 2017

page(s)

29-34

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Differential imprinting and expression of maternal and paternal genomes

30 July 2017

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Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

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A genetic review of complete and partial hydatidiform moles and nonmolar triploidy

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Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set

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Parental origin of triploidy in human fetuses: evidence for genomic imprinting

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Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11

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Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

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Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy

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Evidence against a major role of PEG1/MEST in Silver-Russell syndrome

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gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

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Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

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7 January 2021

Increased parental ages and uniparental disomy 15: a paternal age effect?

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7 January 2021

Confined placental mosaicism and intrauterine fetal growth

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7 January 2021

Confined placental mosaicism

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7 January 2021

Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis

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Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome

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7 January 2021

Severe fetal malformations associated with trisomy 16 confined to the placenta

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7 January 2021

The incidence of uniparental disomy associated with intrauterine growth retardation in a cohort of thirty-five severely affected babies

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7 January 2021

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7 January 2021

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7 January 2021

Do we understand the evolution of genomic imprinting?

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7 January 2021

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

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7 January 2021

Genomic imprinting--defusing the ovarian time bomb.

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7 January 2021

Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation

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7 January 2021

Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus

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7 January 2021

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event

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7 January 2021

Maternal uniparental disomy 14 as a cause of intrauterine growth retardation and early onset of puberty

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7 January 2021

Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)

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7 January 2021

Maternal UPD 20 in a hyperactive child with severe growth retardation

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7 January 2021

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Identifiers

DOI

1 reference

30 July 2017

1 reference