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Volumn 20, Issue 10, 2000, Pages 847-850
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Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p 16.3;q11) translocation
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Author keywords
3:1 segregation; Del(4)(p16); Wolf Hirschhorn syndrome
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Indexed keywords
ARTICLE;
CASE REPORT;
CHROMOSOME 1;
CHROMOSOME 11Q;
CHROMOSOME 15;
CHROMOSOME 16P;
CHROMOSOME 3;
CHROMOSOME BREAKAGE;
CHROMOSOME DELETION 4;
CHROMOSOME DUPLICATION;
CHROMOSOME REARRANGEMENT;
CHROMOSOME SEGREGATION;
CHROMOSOME TRANSLOCATION;
DEVELOPMENTAL DISORDER;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GROWTH RETARDATION;
HUMAN;
MONOSOMY;
NEWBORN;
PRIORITY JOURNAL;
WOLF HIRSCHHORN SYNDROME;
ABNORMALITIES, MULTIPLE;
ADULT;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 4;
FATAL OUTCOME;
FEMALE;
FETAL GROWTH RETARDATION;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INFANT, NEWBORN;
KARYOTYPING;
PREGNANCY;
SYNDROME;
CANIS;
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EID: 0033735875
PISSN: 01973851
EISSN: None
Source Type: Journal
DOI: 10.1002/1097-0223(200010)20:10<847::AID-PD930>3.0.CO;2-O Document Type: Article |
Times cited : (2)
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References (8)
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