(Q41178545)

27 September 2017

title

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

1 reference

27 September 2017

2

Opitz JM

1 reference

27 September 2017

Robin NH

1

1 reference

27 September 2017

Muenke M

series ordinal

3

1 reference

27 September 2017

publication date

1 March 1996

1 reference

American Journal of Medical Genetics Part A

27 September 2017

published in

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27 September 2017

volume

62

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27 September 2017

issue

3

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27 September 2017

page(s)

305-317

1 reference

G syndrome: an unusual family.

27 September 2017

cites work

1 reference

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Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2)

21 January 2018

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G syndrome: a review of the literature and a case report

21 January 2018

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Opitz (BBB/G) syndrome: oral manifestations

21 January 2018

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Total laryngotracheal hypoplasia in a case of G syndrome

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Phenotypic overlap of the BBB and G syndromes

21 January 2018

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

21 January 2018

1 reference

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Sudden death in childhood in a case of the G syndrome.

21 January 2018

1 reference

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Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome

21 January 2018

1 reference

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

21 January 2018

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Velo-cardio-facial syndrome: a review of 120 patients.

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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G syndrome and its otolaryngologic manifestations

21 January 2018

1 reference

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Platelet dysfunction in a patient with the Opitz (BBBG) syndrome

21 January 2018

1 reference

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Apparent Opitz BBBG syndrome with a partial duplication of 5p.

21 January 2018

1 reference

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

21 January 2018

1 reference

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A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expression

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography

21 January 2018

1 reference

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Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

Opitz oculo-genital-laryngeal syndrome (Opitz BBB/G compound syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

BBBG syndrome or Opitz syndrome: new family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

Apparent G syndrome presenting as neck and upper limb dystonia and severe gastroesophageal reflux.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

Discordant expression of the G syndrome in monozygotic twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960329%2962%3A3%3C305%3A%3AAID-AJMG20%3E3.0.CO%3B2-N

10.1002/(SICI)1096-8628(19960329)62:3<305::AID-AJMG20>3.0.CO;2-N

21 January 2018

Identifiers

DOI

1 reference

27 September 2017

1 reference