(Q81640925)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18627037%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis (English)

1 reference

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10 January 2020

7

David L Rimoin

1 reference

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10 January 2020

6

Ralph S Lachman

1 reference

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10 January 2020

author name string

Deborah Krakow

1

1 reference

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10 January 2020

Yasemin Alanay

2

1 reference

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10 January 2020

Lauren P Rimoin

3

1 reference

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10 January 2020

Victoria Lin

4

1 reference

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10 January 2020

William R Wilcox

5

1 reference

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10 January 2020

publication date

1 August 2008

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American Journal of Medical Genetics

10 January 2020

published in

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10 January 2020

volume

146A

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10 January 2020

issue

15

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10 January 2020

page(s)

1917-1924

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Antenatal detection of skeletal dysplasias.

10 January 2020

cites work

1 reference

12 December 2020

Antenatal diagnosis of lethal skeletal dysplasias

1 reference

12 December 2020

Molecular ontogeny of the skeleton

1 reference

12 December 2020

Morphogenesis and dysmorphogenesis of the appendicular skeleton.

1 reference

12 December 2020

Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12).

1 reference

12 December 2020

The birth prevalence rates for the skeletal dysplasias

1 reference

12 December 2020

Second trimester diagnosis of fetal skeletal dysplasias.

1 reference

12 December 2020

Birth prevalence rates of skeletal dysplasias.

1 reference

12 December 2020

Prenatal diagnosis of the skeletal dysplasias.

1 reference

12 December 2020

Epidemiology of osteochondrodysplasias: changing trends due to advances in prenatal diagnosis.

1 reference

12 December 2020

Cesarean delivery for fetal malformations

1 reference

12 December 2020

Prenatal sonographic diagnosis of skeletal dysplasias--a report of the diagnostic and prognostic accuracy in 35 cases.

1 reference

12 December 2020

Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX)

1 reference

12 December 2020

Detection of malformations in chromosomally normal fetuses by routine ultrasound at 12 or 18 weeks of gestation-a randomised controlled trial in 39,572 pregnancies

1 reference

12 December 2020

Nosology and classification of genetic skeletal disorders: 2006 revision

1 reference

12 December 2020

The 20-week scan: beyond biometry and anatomy

1 reference

12 December 2020

Chondrodysplasia punctata and maternal autoimmune disease: a new case and review of the literature

1 reference

12 December 2020

Use of three-dimensional ultrasound imaging in the diagnosis of prenatal-onset skeletal dysplasias

1 reference

12 December 2020

1 reference

12 December 2020

Prenatal sonographic diagnosis of skeletal dysplasias. A report of 47 cases

1 reference

12 December 2020

Defects of human skeletogenesis--models and mechanisms

1 reference

12 December 2020

Molecular-pathogenetic classification of genetic disorders of the skeleton

1 reference

12 December 2020

International nosology and classification of constitutional disorders of bone (2001).

1 reference

12 December 2020

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

1 reference

12 December 2020

Ultrasonographic and radiologic visualization of the developing embryonic skeleton

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.32269

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18627037%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

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10 January 2020

PubMed publication ID

18627037

1 reference