|
Volumn 94, Issue 3-4, 2001, Pages 142-146
|
Molecular and cytogenetic characterisation of a small interstitial de novo 20p13→p12.3 deletion in a patient with severe growth deficit
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ALAGILLE SYNDROME;
ALLELE;
ARTICLE;
CASE REPORT;
CHROMOSOME 20P;
CHROMOSOME BANDING PATTERN;
CHROMOSOME DELETION;
CLINICAL FEATURE;
CYTOGENETICS;
DEVELOPMENTAL DISORDER;
DISEASE COURSE;
FACE DYSMORPHIA;
FLUORESCENCE IN SITU HYBRIDIZATION;
GROWTH DISORDER;
GROWTH RETARDATION;
HAPLOTYPE;
HUMAN;
INFANT;
KARYOTYPE;
MALE;
MOLECULAR GENETICS;
MUSCLE HYPOTONIA;
PRIORITY JOURNAL;
ALLELES;
CHROMOSOME BANDING;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 20;
CONTIG MAPPING;
EUROPEAN CONTINENTAL ANCESTRY GROUP;
FEMALE;
GROWTH DISORDERS;
HAPLOTYPES;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INFANT;
KARYOTYPING;
MALE;
MICROSATELLITE REPEATS;
PEDIGREE;
|
EID: 0035724442
PISSN: 03010171
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (7)
|
References (26)
|