(Q52520470)

2 May 2018

title

Goldenhar, Möbius and hypoglossia-hypodactyly anomalies in a patient: syndrome or association? (English)

1 reference

2 May 2018

author name string

S Preis

1

1 reference

2 May 2018

F Majewski

2

1 reference

2 May 2018

R Hantschmann

3

1 reference

2 May 2018

H Schumacher

4

1 reference

2 May 2018

H G Lenard

5

1 reference

2 May 2018

publication date

1 May 1996

1 reference

2 May 2018

European Journal of Pediatrics

published in

1 reference

2 May 2018

volume

155

1 reference

2 May 2018

issue

5

1 reference

2 May 2018

page(s)

385-389

1 reference

2 May 2018

https://scigraph.springernature.com/pub.10.1007/s004310050423

exact match

0 references

cites work

Möbius sequence: further in vivo support for the subclavian artery supply disruption sequence.

1 reference

12 December 2020

Monozygotic twinning and structural defects

1 reference

12 December 2020

Syndrome of anotia, facial paralysis, and congenital heart disease

1 reference

12 December 2020

Familial occurrence of malformations possibly attributable to vascular abnormalities

1 reference

12 December 2020

Moebius syndrome in a child and extremity defect in her father

1 reference

12 December 2020

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

1 reference

12 December 2020

Congenital ophthalmoplegia in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome). A clinicopathologic study and review of the literature

1 reference

12 December 2020

Vascular pathogenesis of transverse limb reduction defects

1 reference

12 December 2020

Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetics of Mobius syndrome

1 reference

12 December 2020

Studies of malformation syndromes of man XXXXI B: Nosologic studies in the Hanhart and the Möbius syndrome

1 reference

12 December 2020

Vascular pathogenesis of unilateral craniofacial defects

1 reference

12 December 2020

Intracranial lipomas, hydrocephalus and other CNS anomalies in oculoauriculo-vertebral dysplasia (Goldenhar-Gorlin syndrome)

1 reference

12 December 2020

Aglossia-adactylia syndrome (special emphasis on the inheritance pattern).

1 reference

12 December 2020

Microtia and associated anomalies: statistical analysis

1 reference

12 December 2020

The pathogenesis of the first and second branchial arch syndrome

1 reference

12 December 2020

Congenital cardiac, pulmonary, and vascular malformations in oculoauriculovertebral dysplasia

1 reference

12 December 2020

Poland anomaly with unusual associated anomalies: case report of an apparent disorganized defect

1 reference

12 December 2020

Moebius sequence and prenatal brainstem ischemia.

1 reference

12 December 2020

Familial liability to intrauterine vascular impairments

1 reference

12 December 2020

The syndrome of ankyloglossia superior

1 reference

12 December 2020

1 reference

12 December 2020

Möbius syndrome: evidence for a vascular etiology.

1 reference

12 December 2020

OCULOAURICULOVERTEBRAL DYSPLASIA.

1 reference

12 December 2020

Disruption sequences: embryonic vascular accident or blastogenic disruption sequence?

1 reference

12 December 2020

Genetic aspects of hemifacial microsomia

1 reference

12 December 2020

Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients

1 reference

12 December 2020

Anotia, facial paralysis, and heart disease

1 reference

12 December 2020

Prenatal cocaine exposure and fetal vascular disruption.

1 reference

12 December 2020

Developmental field theory and observations--accidental progress?

1 reference

12 December 2020

A "community" of face-limb malformation syndromes

1 reference

12 December 2020

Anotia, facial paralysis, heart abnormalities: specific triad or variant of Goldenhar syndrome?

1 reference

12 December 2020

Craniofacial changes in hemifacial microsomia

1 reference

12 December 2020

Severe axial anomalies in the oculo-auriculo-vertebral (Goldenhar) complex.

1 reference

12 December 2020

1 reference

12 December 2020

Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome ?A pathogenetic hypothesis

1 reference

12 December 2020

Hemifacial microsomia and variants: pedigree data

1 reference

12 December 2020

Developmental anomalies in mice resulting from action of the gene, disorganization, a semi-dominant lethal.

1 reference

12 December 2020

The association of facial palsy and/or sensorineural hearing loss in patients with hemifacial microsomia

1 reference

12 December 2020

Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation

1 reference

12 December 2020

The Triad of Anotia, Facial Paralysis, and Cardiac Anomaly Not Due To Thalidomide

1 reference

12 December 2020

1 reference

12 December 2020

The first arch syndrome

1 reference

12 December 2020

Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancy

1 reference

12 December 2020

Vascular origin of Poland syndrome? A comparative rheographic study of the vascularisation of the arms in eight patients

1 reference

12 December 2020

CONGENITAL MALFORMATIONS AND MATERNAL DIABETES

1 reference

12 December 2020

Hypoglossia-hypodactylia syndrome with jejunal atresia in an infant of a diabetic mother

1 reference

12 December 2020

Poland anomaly with a limb body wall disruption defect.

1 reference

12 December 2020

[The aglossia-adactylia syndrome]

1 reference

12 December 2020

Identifiers

DOI

10.1007/S004310050423

1 reference

2 May 2018

release_vhguq6d2k5bp5ffanybz24bq3m

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vhguq6d2k5bp5ffanybz24bq3m

24 November 2022

mapped directly with Wikidata item

1 reference

2 May 2018