(Q37709820)

22 August 2017

Trisomy 13, 18, 21, Triploidy and Turner syndrome: the 5T's. Look at the hands (English)

1 reference

22 August 2017

1 reference

5

1 reference

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31 May 2020

author name string

G Witters

1

1 reference

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31 May 2020

J Van Robays

2

1 reference

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31 May 2020

C Willekes

3

1 reference

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31 May 2020

A Coumans

4

1 reference

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31 May 2020

W Gyselaers

6

1 reference

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31 May 2020

J P Fryns

7

1 reference

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31 May 2020

publication date

1 January 2011

1 reference

22 August 2017

7

1 reference

Facts, Views & Vision in ObGyn

inferred from page(s)

published in

1 reference

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31 May 2020

volume

3

1 reference

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31 May 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24753843%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

page(s)

15-21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24753843%20AND%20SRC:MED&resulttype=core&format=json

Holoprosencephaly due to numeric chromosome abnormalities

31 May 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Counseling in isolated mild fetal ventriculomegaly

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Turner syndrome and clinical treatment.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Sonographic detection of trisomy 13 in the first and second trimesters of pregnancy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Functional analysis of mutations in TGIF associated with holoprosencephaly

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Clinical practice in Turner syndrome.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

The role of the second trimester genetic sonogram in screening for fetal Down syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Prenatal ultrasound diagnosis of Down syndrome. After major malformations, soft markers, nuchal translucency and skeletal signs, a new vascular sign?

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

First-trimester screening for chromosomal abnormalities

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Down syndrome and genetics - a case of linked histories.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Second-trimester sonography and trisomy 18: the significance of isolated choroid plexus cysts after an examination that includes the fetal hands

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Second-trimester sonography and trisomy 18.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

A case of partial mole and atypical type I triploidy associated with severe HELLP syndrome at 18 weeks' gestation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Second trimester ultrasound screening for chromosomal abnormalities

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Autoimmune thyroid syndrome in women with Turner's syndrome--the association with karyotype

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Sonographic markers of fetal trisomies: second trimester.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Ultrasound findings and multiple marker screening in trisomy 18.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Choroid plexus cysts: not associated with Down syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Trisomy 13 syndrome: prenatal US findings in a review of 33 cases

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Intrauterine diagnosis of sex chromosome aneuploidy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Effects of triploidy on early human development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Second trimester ultrasonography may identify 77 to 97% of fetuses with trisomy 18.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Detection of chromosomal abnormalities, an outcome of ultrasound screening. The Eurofetus Team

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Screening for trisomy 18 by maternal age, fetal nuchal translucency, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

First-trimester or second-trimester screening, or both, for Down's syndrome

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

First-trimester screening for fetal triploidy at 11 to 14 weeks: a role for fetal biometry.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Aberrant right subclavian artery as a new cardiac sign in second- and third-trimester fetuses with Down syndrome.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

The genetic sonogram: a method of risk assessment for Down syndrome in the second trimester.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

One-stop clinic for assessment of risk for trisomy 21 at 11-14 weeks: a prospective study of 15 030 pregnancies

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Clinical significance of fetal choroid plexus cysts

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3991414

Prenatal diagnosis of Turner syndrome: report on 69 cases

1 September 2018

1 reference

12 December 2020

Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome

1 reference

12 December 2020

Prenatal diagnosis of trisomy 13: analysis of 28 cases

1 reference

12 December 2020

Decreased first trimester PAPP-A is a predictor of adverse pregnancy outcome

1 reference

12 December 2020

Karyotyping of fetuses with isolated choroid plexus cysts is not justified in an unselected population

1 reference

12 December 2020

Sonographic screening for trisomy 13 at 11 to 13(+6) weeks of gestation

1 reference

12 December 2020

First-trimester sonographic diagnosis of holoprosencephaly: value of the "butterfly" sign

1 reference

12 December 2020

Trisomy 18 presenting with severe limb deformations

1 reference

12 December 2020

A first trimester trisomy 13/trisomy 18 risk algorithm combining fetal nuchal translucency thickness, maternal serum free beta-hCG and PAPP-A

1 reference

12 December 2020

Prospective first-trimester screening for trisomy 21 in 30,564 pregnancies

1 reference

12 December 2020

Nasal bone hypoplasia in trisomy 21 at 15-22 weeks' gestation

1 reference

12 December 2020

Triploidy in a twin pregnancy: small placenta volume as an early sonographical marker

1 reference

12 December 2020

Relative risk of abnormal karyotype in fetuses found to have an atrioventricular septal defect (AVSD) on fetal echocardiography

1 reference

12 December 2020

Fetal nose bone length: a marker for Down syndrome in the second trimester

1 reference

12 December 2020

First-trimester screening for trisomies 21 and 18

1 reference

12 December 2020

Is second-trimester genetic amniocentesis for trisomy 18 ever indicated in the presence of a normal genetic sonogram?

1 reference

12 December 2020

Absence of nasal bone in fetuses with trisomy 21 at 11–14 weeks of gestation: an observational study

1 reference

12 December 2020

Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe

1 reference

12 December 2020

Aberrant right subclavian artery at 16 to 23 + 6 weeks of gestation: a marker for chromosomal abnormality

1 reference

12 December 2020

Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases

1 reference

12 December 2020

Prenatal Diagnosis of Craniomaxillofacial Malformations: A Characterization of Phenotypes in Trisomies 13, 18, and 21 by Ultrasound and Pathology

1 reference

12 December 2020

Isolated sonographic markers for detection of fetal Down syndrome in the second trimester of pregnancy

1 reference

12 December 2020

Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004

1 reference

12 December 2020

Increased nuchal translucency thickness in thrombocytopenia-absent-radius syndrome

1 reference

12 December 2020

Screening for triploidy by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 10-14 weeks of gestation

1 reference

12 December 2020

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

1 reference

12 December 2020

Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24753843%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

PubMed publication ID

24753843

1 reference