The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications

American Journal of Human Genetics

Volumn 58, Issue 4, 1996, Pages 785-796

  Floridia, Giovanna ^b   Piantanida, Mauro ^b   Minelli, Antonella ^b   Dellavecchia, Claudia ^b   Bonaglia, Clara ^b   Rossi, Elena ^b   Gimelli, Giorgio ^b   Croci, Gianfranco ^b   Franchi, Fabrizia ^b   Gilgenkrantz, Simone ^b   Grammatico, Paola ^b   Dalprá, Leda ^b   Wood, Stephen ^b   Danesino, Cesare ^b   Zuffardi, Orsetta ^a  

^a UNIVERSITY OF PAVIA   (Italy)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DEFENSIN;

ANAPHASE; ARTICLE; CENTROMERE; CHROMOSOME 8P; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CYTOGENETICS; DICENTRIC CHROMOSOME; DNA POLYMORPHISM; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MEIOSIS; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; TELOMERE;

ABNORMALITIES, MULTIPLE; BRAIN; CENTROMERE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 8; CROSSING OVER, GENETIC; FACE; FEMALE; HUMANS; MALE; MEIOSIS; MENTAL RETARDATION; MODELS, GENETIC; MULTIGENE FAMILY; POLYMORPHISM, GENETIC; SYNDROME;

EID: 19144369894     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Barber JCK, James RS, Patch C, Temple IK (1994) Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8. Am J Med Genet 50:296-299
2. Bondeson ML, Dahl N, Malmgren H, Kleijer WJ, Tönnensen T, Carlberg BM, Pettersson U (1995) Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome. Hum Mol Genet 4:615-621
3. Cheng S-D, Spinner NB, Zackai EH, Knoll JHM (1994) Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients. Am J Hum Genet 55:753-759
4. Cohen D, Chumakov I, Weissenbach J (1993) A first-generation physical map of the human genome. Nature 366:698-701
5. Wright EC, Goldgar DE, Fain PR, Barker DF, Skolnick MH (1990) A genetic map of human chromosome 17p. Genomics 7:103-109
6. Yen PH, Li XM, Tsai SP, Johnson C, Mohandas T, Shapiro LJ (1990) Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements. Cell 61:603-610