Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.

F Giraudeau; L Taine; V Biancalana; B Delobel; H Journel; C Missirian; D Lacombe; D Bonneau; P Parent; D Aubert; Y Hauck; M F Croquette; A Toutain; M G Mattei; H A Loiseau; A David; Gilles Vergnaud

doi:10.1136/jmg.38.2.121

Journal Articles Journal of Medical Genetics Year : 2001

Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.

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F Giraudeau

Function : Author

L Taine

Function : Author

V Biancalana

Function : Author

Institut de Génétique et de Biologie Moléculaire et Cellulaire

B Delobel

Function : Author

Centre de Génétique Chromosomique

H Journel

Function : Author

C Missirian

Function : Author

Département de génétique médicale [Hôpital de la Timone - APHM]

D Lacombe

Function : Author

Service de génétique médicale

D Bonneau

Function : Author

Mitochondrie : Régulations et Pathologie

Service de génétique

P Parent

Function : Author

Centre Interdisciplinaire de Nanoscience de Marseille

D Aubert

Function : Author
PersonId : 904836

Y Hauck

Function : Author

Institut de génétique et microbiologie [Orsay]

M F Croquette

Function : Author

Echanges Côte-Large

A Toutain

Function : Author
PersonId : 825028
ORCID : 0000-0002-5999-5300
IdRef : 08130871X

Service de génétique [Tours]

M G Mattei

Function : Author

Parc Naturel National Loire-Anjou-Touraine

H A Loiseau

Function : Author

CHU Bordeaux

A David

Function : Author

MLab

Gilles Vergnaud

Function : Author
PersonId : 2910
IdHAL : gilles-vergnaud
ORCID : 0000-0003-0913-194X
IdRef : 034239464

École Nationale Supérieure de Techniques Avancées

Institut de génétique et microbiologie [Orsay]

CV

Domains

Life Sciences [q-bio] Human health and pathology

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v038p00121.pdf (184.33 Ko)

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Julien Caugant : Connect in order to contact the contributor

https://ensta-paris.hal.science/hal-01158343

Submitted on : Thursday, November 16, 2023-11:53:57 AM

Last modification on : Friday, April 19, 2024-4:18:58 PM

Dates and versions

hal-01158343 , version 1 (16-11-2023)

Identifiers

HAL Id : hal-01158343 , version 1
DOI : 10.1136/jmg.38.2.121
PUBMED : 11288712
PUBMEDCENTRAL : PMC1734816

Cite

F Giraudeau, L Taine, V Biancalana, B Delobel, H Journel, et al.. Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.. Journal of Medical Genetics, 2001, 38 (2), pp.121-5. ⟨10.1136/jmg.38.2.121⟩. ⟨hal-01158343⟩

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Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.

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