A GIRL WITH G-SYNDROME AND AGENESIS OF THE CORPUS-CALLOSUM

Giovanni Neri; Maurizio Genuardi; G Natoli; P Costa; G Maggioni

doi:10.1002/ajmg.1320280204

A GIRL WITH G-SYNDROME AND AGENESIS OF THE CORPUS-CALLOSUM

Giovanni Neri, Maurizio Genuardi, G Natoli, P Costa, G Maggioni

Risultato della ricerca: Contributo in rivista › Articolo in rivista

Abstract

We report on a female patient with G syndrome. The clinical expression is relatively severe and includes 2 manifestations not previously reported, ie, agenesis of the corpus callosum and umbilical hernia. These new findings support the notion that there is a developmental defect of the midline as the basis of the G syndrome.

Lingua originale	English
pagine (da-a)	287-291
Numero di pagine	5
Rivista	American Journal of Medical Genetics
Volume	28
DOI	https://doi.org/10.1002/ajmg.1320280204
Stato di pubblicazione	Pubblicato - 1987

Keywords

syndrome

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10.1002/ajmg.1320280204

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title = "A GIRL WITH G-SYNDROME AND AGENESIS OF THE CORPUS-CALLOSUM",

abstract = "We report on a female patient with G syndrome. The clinical expression is relatively severe and includes 2 manifestations not previously reported, ie, agenesis of the corpus callosum and umbilical hernia. These new findings support the notion that there is a developmental defect of the midline as the basis of the G syndrome.",

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author = "Giovanni Neri and Maurizio Genuardi and G Natoli and P Costa and G Maggioni",

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AU - Neri, Giovanni

AU - Genuardi, Maurizio

AU - Natoli, G

AU - Costa, P

AU - Maggioni, G

PY - 1987

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N2 - We report on a female patient with G syndrome. The clinical expression is relatively severe and includes 2 manifestations not previously reported, ie, agenesis of the corpus callosum and umbilical hernia. These new findings support the notion that there is a developmental defect of the midline as the basis of the G syndrome.

AB - We report on a female patient with G syndrome. The clinical expression is relatively severe and includes 2 manifestations not previously reported, ie, agenesis of the corpus callosum and umbilical hernia. These new findings support the notion that there is a developmental defect of the midline as the basis of the G syndrome.

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UR - http://hdl.handle.net/10807/220285

U2 - 10.1002/ajmg.1320280204

DO - 10.1002/ajmg.1320280204

M3 - Article

SN - 0148-7299

VL - 28

SP - 287

EP - 291

JO - American Journal of Medical Genetics

JF - American Journal of Medical Genetics

ER -

A GIRL WITH G-SYNDROME AND AGENESIS OF THE CORPUS-CALLOSUM

Abstract

Keywords

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