Pachytene analysis in males heterozygous for a familial translocation (9;12;13) (q22;q22;q32) ascertained through a child with partial trisomy 9

Cytogenetics and Cell Genetics

Volumn 47, Issue 3, 1988, Pages 160-166

  Johannisson, R ^a   Lohrs U ^a   Passarge, E ^b  

^a UNIVERSITY OF LÜBECK   (Germany)

^b UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 9; CYTOLOGY; FEMALE; HEREDITY; HISTOLOGY; HUMAN; MALE; MALE INFERTILITY; MEIOSIS; PACHYTENE; PARTIAL TRISOMY 9; PEDIGREE; ULTRASTRUCTURE;

CASE REPORT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HETEROZYGOTE; HUMAN; INFANT, NEWBORN; KARYOTYPING; MALE; MEIOSIS; PEDIGREE; SPERMATOCYTES; SUPPORT, NON-U.S. GOV'T; TESTIS; TRANSLOCATION (GENETICS); TRISOMY;

EID: 0023706128     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000132537     Document Type: Article

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