(Q74806035)

English

Further delineation of the Opitz G/BBB syndrome: report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature

scientific article published on 01 July 1998

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference

Europe PubMed Central

Further delineation of the Opitz G/BBB syndrome: report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

congenital heart disease

1 reference

based on heuristic

inferred from title

bladder exstrophy

1 reference

based on heuristic

inferred from title

author name string

Z Jacobson

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

J Glickstein

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

T Hensle

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

R W Marion

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

publication date

1 July 1998

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

78

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

294-299

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

G syndrome: an unusual family.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Total laryngotracheal hypoplasia in a case of G syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The Opitz syndrome: a new designation for the clinically indistinguishable BBB and G syndromes.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Genetics of atrial septal defect

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Endocrinological studies in the hypertelorism-hypospadias (BBB) syndrome.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Ring chromosome 22 karyotype in a patient with Opitz (BBBG) syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Phenotypic overlap of the BBB and G syndromes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The G syndrome of dysphagia, ocular hypertelorism and hypospadias

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The hypertelorism-hypospadias syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Male to male transmission of the G syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The G and BBB syndromes: Case presentations, genetics, and nosology

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Studies of malformation syndromes of man VB: the hypertelorism-hypospadias (BBB) syndrome. Case report and review

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The G syndrome: a case report

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Prenatal diagnosis of Opitz (BBB) syndrome in the second trimester by ultrasound detection of hypospadias and hypertelorism.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Brain magnetic resonance imaging findings in the Opitz G/BBB syndrome: extension of the spectrum of midline brain anomalies

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Hypertelorism-Hypospadias Syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The G syndrome. A four-generation family study

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

The telecanthus-hypospadias syndrome.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Distal deletion of chromosome 13 in a child with the "opitz" GBBB syndrome.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

BBBG syndrome or Opitz syndrome: new family

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Opitz GBBB syndrome: chromosomal evidence of an X-linked form.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Further delineation of the G syndrome: a manageable genetic cause of infantile dysphagia

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Discordant expression of the G syndrome in monozygotic twins.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C294%3A%3AAID-AJMG18%3E3.0.CO%3B2-A

21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19980707)78:3<294::AID-AJMG18>3.0.CO;2-A

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677070%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q74806035&oldid=1900030938"