Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome

American Journal of Medical Genetics

Volumn 69, Issue 2, 1997, Pages 166-168

  Cormier Daire, Valérie ^a   Le Merrer, Martine ^a   Gigarel, Nadine ^a   Morichon, Nicole ^a   Prieur, Marguerite ^a   Lyonnet, Stanislas ^a   Vekemans, Michel ^a   Munnich, Arnold ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

isochrome 12p; Pallister Killian syndrome; prezygotic origin

Indexed keywords

ALLELE; ARTICLE; CASE REPORT; CHROMOSOME 12P; CHROMOSOME ANALYSIS; CLINICAL FEATURE; FEMALE; HUMAN; HUMAN CELL; ISOCHROMOSOME; MEIOSIS; NEWBORN; NONDISJUNCTION; PALLISTER KILLIAN SYNDROME; PRIORITY JOURNAL; SKIN FIBROBLAST; TETRASOMY;

ABNORMALITIES, MULTIPLE; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; GENETIC MARKERS; HUMANS; INFANT; ISOCHROMOSOMES; MENTAL RETARDATION; MICROSATELLITE REPEATS; PEDIGREE; SKIN PIGMENTATION; SYNDROME;

EID: 0031049563     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970317)69:2<166::AID-AJMG9>3.0.CO;2-N     Document Type: Article

References (7)

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