45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationships (Q36265957)

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English	45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationships	scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationships (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1

object named as

Gareth Baynam

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Jack Goldblatt

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

publication date

1 September 2009

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Journal of maxillofacial and oral surgery

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

279-282

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

OCULOAURICULOVERTEBRAL DYSPLASIA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Intracytoplasmic sperm injection may increase the risk of imprinting defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Assisted reproductive technologies and monozygous twins: implications for future study and clinical practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Microtia: a microform of hemifacial microsomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Identical twins and in vitro fertilization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Goldenhar syndrome and overlapping dysplasias, in vitro fertilisation and ovopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Goldenhar complex in discordant monozygotic twins: a case report and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Retinoic acid embryopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Severe manifestations of oculoauriculovertebral spectrum in a cocaine exposed infant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

30 September 2017

Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

29 June 2018

46,XY/47,XY, + 17p + mosaicism in amniocytes associated with fetal abnormalities despite normal fetal blood karyotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

29 June 2018

Probably monozygotic twins with discordance for Goldenhar syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

29 June 2018

Sex chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

29 June 2018

Survival probability of human conceptions from fertilization to term

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

29 June 2018

Monozygotic twinning and structural defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

29 June 2018

Histone acetylation dependent allelic expression imbalance of BAPX1 in patients with the oculo-auriculo-vertebral spectrum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

22 September 2018

Demographic and reproductive factors associated with hemifacial microsomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

22 September 2018

Is hemifacial microsomia linked to multiple maternities?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

22 September 2018

Hemifacial microsomia and abnormal chromosome 22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

22 September 2018

Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

22 September 2018

Variability versus "incidental findings" in the first and second branchial arch syndrome: unilateral variants with anophthalmia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454233

21 October 2018

Ultrasonic assessment of the high rate of human multiple pregnancy in the first trimester

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The first and second branchial arch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Goldenhar anomaly in one of triplets derived from in vitro fertilization

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Goldenhar anomaly in one triplet derived from intracytoplasmic sperm injection (ICSI)

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgG subclass response and opsonization of Streptococcus pneumoniae after vaccination of healthy adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathogenesis of the first and second branchial arch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Goldenhar's syndrome: discordance in monozygotic twins and unusual anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Etiologic heterogeneity in the oculoauriculovertebral syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monozygotic twinning in the human is associated with the zona pellucida architecture

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family with dominant oculoauriculovertebral spectrum

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Birthweight in dizygotic twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Case of epibulbar dermolipoma with unilateral facial malformation in an uniovular twin]

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assisted reproductive therapies and imprinting disorders--a preliminary British survey

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical and cytogenetic study of fifteen patients with 45,X/46XY gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal blood sampling demonstrating chimerism in monozygotic twins discordant for sex and tissue karyotype (46,XY and 45,X)

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal abnormality (Goldenhar syndrome) occurring in one of triplet infants derived from in vitro fertilization with possible monozygotic twinning

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Discordant Franceschetti-Goldenhar syndrome in 2 monozygotic twins]

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution on the clinical aspects of the Goldenhar syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Goldenhar's syndrome with associated malformations]

1 reference

https://pubmed.ncbi.nlm.nih.gov/23139526

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12663-009-0068-X

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

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