The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte

Human Genetics

Volumn 88, Issue 4, 1992, Pages 482-483

  Simi, P ^a   Ceccarelli, M ^a   Barachini, A ^a   Floridia, G ^b   Zuffardi, O ^b  

^a UNIVERSITY OF PISA   (Italy)

^b UNIVERSITY OF PAVIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; FEMALE; HUMAN; KARYOTYPE; MALE; MEIOSIS; NONDISJUNCTION; PRIORITY JOURNAL; PROGENY; SPERMATOCYTE; TRISOMY;

CASE REPORT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; HETEROZYGOTE DETECTION; HUMAN; KARYOTYPING; LYMPHOCYTES; MALE; MEIOSIS; NONDISJUNCTION, GENETIC; SPERMATOCYTES; TRANSLOCATION (GENETICS);

EID: 0026547380     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00215688     Document Type: Article

References (7)

1. The 11q;22q translocation: a European collaborative analysis of 43 cases
2. The 11q22q translocation: a collaborative study of 20 new cases and analysis of 110 families
3. Further studies on bivalent chiasma frequency in human males with normal karyotypes
4. Further studies on chiasma distribution and interference in the human male
5. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3∶1 segregation in first meiosis
6. Characterization of the supernumerary chromosome in cat eye syndrome
7. The “cat-eye-syndrome”: dicentric small marker chromosome probably derived from a no. 22 (tetrasomy 22pter-to q11) associated with a characteristic phenotype: report of 11 patients and delineation of the clinical picture