Duplication/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Clinical cytogenetics;Ferguson-Smith,1966
2. Inherited pericentric inversion of chromosome No. 4;Wilson;Am. J. Hium. Genet.,1970
3. Patau's syndrome with D1 duplication-deficiency derived from a maternal D group pericentric inversion
4. Inherited pericentric inversion of a group D (13–15) chromosome;Surana;J. Med. Genet.,1972
5. Chromosome preparations of leukocytes cultured from human peripheral blood;Moorhead;Exp. Cell Res.,1960
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1. Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations;Clinical Genetics;2008-04-23
2. Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers;Clinical Genetics;2008-04-23
3. Screening of subtelomeric rearrangements in autistic disorder: Identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2006
4. Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13;American Journal of Medical Genetics Part A;2005
5. Segregation of inverted chromosome 13 in families ascertained through liveborn recombinant offspring;American Journal of Medical Genetics;1987-05
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