Congenital hyperinsulinism and mosaic abnormalities of the ploidy

Journal of Medical Genetics

Volumn 43, Issue 3, 2006, Pages 248-254

  Giurgea, Irina ^a   Sanlaville, D ^a   Fournet, J C ^a   Sempoux, C ^b   Bellanne Chantelot C ^c   Touati, G ^a   Hubert, L ^a   Groos, M S ^a   Brunelle, F ^a   Rahier, J ^b   Henquin, J C ^b   Dunne, M J ^d   Jaubert, F ^a   Robert, J J ^a   Nihoul Fekete C ^a   Vekemans, M ^a   Junien, C ^a   De Lonlay, P ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

^c HÔPITAL SAINT ANTOINE   (France)

^d UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; ARTICLE; BECKWITH WIEDEMANN SYNDROME; BLOOD GROUP TYPING; CASE REPORT; COMORBIDITY; DNA POLYMORPHISM; ELECTROPHYSIOLOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENOME; GENOTYPE; HISTOPATHOLOGY; HUMAN; HYPOGLYCEMIA; INSULINOMA; KARYOTYPE; MALE; MICROFLUOROMETRY; MOSAICISM; NEWBORN; PANCREAS TUMOR; PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PLOIDY; PRIORITY JOURNAL; TRIPLOIDY; UNIPARENTAL DISOMY;

ABNORMALITIES; CHROMOSOME ABERRATIONS; FEMALE; HUMANS; HYPERINSULINISM; INFANT, NEWBORN; MALE; MOSAICISM; PLOIDIES;

EID: 33645112746     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2005.034116     Document Type: Article

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