(Q41653858)

6 October 2017

1 reference

title

Growth effects of uniparental disomies and the conflict theory of genomic imprinting (English)

1 reference

6 October 2017

Hurst LD

1

1 reference

PubMed ID

9385840

6 October 2017

McVean GT

series ordinal

2

1 reference

6 October 2017

1 November 1997

1 reference

6 October 2017

1 reference

6 October 2017

13

1 reference

6 October 2017

436-443

1 reference

6 October 2017

11

1 reference

Parent-Offspring Conflict

6 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Genomic imprinting in mammalian development: a parental tug-of-war

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental maternal disomy 6 in a renal transplant patient

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Human PEG1/MEST, an imprinted gene on chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy for chromosome 14.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Genetic conflicts in human pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Genomic imprinting related to prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

An audit of trisomy 16 in man.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Human maternal uniparental disomy for chromosome 16 and fetal development

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

An imprinted gene(s) for diabetes?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

A case of paternal uniparental disomy for chromosome 11.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Paternal uniparental disomy for chromosome 14: a case report and review

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

A clinical and molecular study of mosaicism for trisomy 17.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Exclusively paternal X chromosomes in a girl with short stature

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Imprinted genes have few and small introns

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Genomic imprinting of Mash2, a mouse gene required for trophoblast development

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy 7 in Silver-Russell syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q)

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy of chromosome 13 in a phenotypically normal child

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Distinct phenotype in maternal uniparental disomy of chromosome 14.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy for chromosome 14

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental disomy with normal phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Case report: uniparental disomy 16 in association with congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Early embryonic failure associated with uniparental disomy for human chromosome 21

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Fortuitous detection of uniparental isodisomy of chromosome 6.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Paternal uniparental disomy for chromosome 6 causes transient neonatal diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Uniparental isodisomy 6 associated with deficiency of the fourth component of complement

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Transient neonatal diabetes mellitus in sibs

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Confined placental mosaicism for trisomy 2 with intrauterine growth retardation and severe oligohydramnios in the absence of uniparental disomy in the fetus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2897%2901273-0

7 January 2021

10.1016/S0168-9525(97)01273-0

Identifiers

DOI

1 reference

6 October 2017

1 reference

PubMed ID

9385840