Interchromosomal insertions: Identification of five cases and a review

Human Genetics

Volumn 107, Issue 5, 2000, Pages 415-432

  Van Hemel, J O ^a   Eussen, H J ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CONGENITAL HEART MALFORMATION; DIAGNOSTIC ACCURACY; DISEASE CARRIER; FAMILIAL DISEASE; GENETIC RISK; HUMAN; INCIDENCE; INHERITANCE; INSERTIONAL CHROMOSOME TRANSLOCATION; MENTAL DEFICIENCY; MICROCEPHALY; PHENOTYPE; PRIORITY JOURNAL; PROGENY; PSYCHOMOTOR RETARDATION; REVIEW; SEGREGATION ANALYSIS; SPONTANEOUS ABORTION; TRISOMY;

ABNORMALITIES, MULTIPLE; ABORTION, SPONTANEOUS; ADULT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN; DNA TRANSPOSABLE ELEMENTS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; PEDIGREE; PREGNANCY; SEQUENCE DELETION; TRANSLOCATION, GENETIC;

EID: 0034537280     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390000398     Document Type: Review

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31. Partial proximal trisomy of the long arm of chromosome 5(q13→q22) resulting from maternal insertion der ins(10;5)
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58. Inverted insertion of chromosome 7q and ectrodactyly
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