(Q73715641)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

A pilot study of the possible role of familial defects in anticoagulation as a cause for terminal limb reduction malformations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

A G Hunter

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 March 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

197-204

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

Vascular pathogenesis of transverse limb reduction defects

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

The vascular pathogenesis of gastroschisis: intrauterine interruption of the omphalomesenteric artery

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

CONGENITAL INTESTINAL ATRESIA OBSERVATIONS ON ITS ORIGIN

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Vascular pathogenesis of unilateral craniofacial defects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Monozygotic twinning and structural defects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Protein C in thromboembolic disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Inherited resistance to activated protein C is corrected by anticoagulant cofactor activity found to be a property of factor V.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Thyropathic endemic dystrophy in an area of the Argeş Valley

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Antiphospholipid (Hughes') syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Homocysteinemia: association of a metabolic disorder with vascular disease and thrombosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Increased fetal loss in women with heritable thrombophilia.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Thrombophilia and fetal loss

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Pregnancy Loss in the Antiphospholipid-Antibody Syndrome — A Possible Thrombogenic Mechanism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Activated protein C resistance can be associated with recurrent fetal loss

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Fetal carriers of the factor V Leiden mutation are prone to miscarriage and placental infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

The relation of aberrant vasculogenesis to skeletal malformation in the hamster fetus

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Peromelia, ipsilateral subclavian atresia, coarctation, and aneurysms of the aorta resulting from intrauterine vascular occlusion

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Vascular pathogenesis of limb defects. I. Radial artery anatomy in radial aplasia.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Twin embolization syndrome: prenatal sonographic detection and significance

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Uterine trauma and limb defects.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Limb reduction defects in fetuses with homozygous alpha-thalassaemia-1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Homozygous protein S deficiency in an infant with purpura fulminans

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Low protein C in the neonatal period

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Plasma Protease Inhibitors in Premature Infants: Influence of Gestational Age, Postnatal Age, and Health Status

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

Polymorphism for mutation of cytosine to thymine at location 677 in the methylenetetrahydrofolate reductase gene is associated with recurrent early fetal loss

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570305.X

7 January 2021

10.1034/J.1399-0004.2000.570305.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782926%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference