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Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.
Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].
Show details- Same entry as in 01p340,05p130 (Boue and Gallano, 1984).
- Boue A, Gallano P: A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses. Prenat. Diag. 4:45-67, 1984. [PubMed: 6463033]inv(17)(p11q25).Aberration: Inversion pericentricNo band
- Docherty Z, Hulten M A, Honeyman M M: De novo tandem duplication 17p11 to cen. J. Med. Genet. 20:138-142, 1983. [PMC free article: PMC1049020] [PubMed: 6842549]46,XX,dup(17p11).&46,XX,dic(17)(pter -> q111::p12 -> qter)mat.Aberration: Dicentric chromosomeNo band
- FitzSimmons J, Wapner R J, Jackson L G: Repeated pregnancy loss. AJMG 16:7-13, 1983. [PubMed: 6638072]46,XX,t(1;17)(17pter -> 17p11::1pter -> 1qter)del(17qter -> 17p11:).Aberration: Simple translocationNo band
- Kotzot D, Martinez M-J, Bagci G, Basaran S, Baumer A, Binkert F, Brecevic L, Castellan C, Chrzankowska K, Dutly F, Gutkowska A, Karauzum S B, Krajewska-Walasek M, Luleci G, Miny P, Riegel M, Schuffenhauer S, Seidel H, Schinzel A.: Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications. J. Med. Genet. 37:281-286, 2000. [PMC free article: PMC1734569] [PubMed: 10745046]Case 18:46,XX,dup(17)(p11p13)patAberration: DuplicationChromosomal Aneuploidy: 17p+
- Martsolf J T, Larson L, Jalal S M, Wasdahl W A, Miller R, Kukolich M K: Complete trisomy 17p. A relatively new syndrome. Ann. Genet. 31:172-174, 1988. [PubMed: 3066280]46,XX,dup(17)(17qter -> 17p13::17p13 -> 17p11).Patient had MCA/MR and died at the age of 10 months following surgery.Aberration: DuplicationChromosomal Aneuploidy: 17p+No band
- Moghe M, Patel Z M, Peter J J, Ambani L M: Cytogenetic studies in a selected group of mentally retarded children. Hum. Genet. 58:184-187, 1981. [PubMed: 6456981]Patient RD was 6 months old.46,XY,del(17)(qter -> p11).Aberration: Terminal deletionNo band
- Patil S R, Bartley J A: Interstitial deletion of the short arm of chromosome 17. Hum. Genet. 67:237-238, 1984. [PubMed: 6745947]Patient A.S. was 4 years old and no major malformations were present but was moderately mentally retarded.46,XX,del(17)(p11).Aberration: Interstitial deletionNo band
- Wiktor A, Van Dyke D L, Weiss L: Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1). AJMG 45:22-24, 1993. [PubMed: 8418653]Case B90-9853.mos46,XX/47,XX,+r(X)(p11q11)/47,XX,r(17)(p11q11)/48,XX,+r(X)(p11q11),+r(17)(p11q11).The patient had familial NF1, short stature, developmental delay and the de novo chromosome abnormality.Aberration: Ring chromosomeMIM#: 162200Index Terms: Neurofibromatosis ... type 1No band
- 17p110 - Chromosomal Variation in Man17p110 - Chromosomal Variation in Man
- RecName: Full=Cysteine desulfurase, mitochondrial; AltName: Full=tRNA-splicing p...RecName: Full=Cysteine desulfurase, mitochondrial; AltName: Full=tRNA-splicing protein SPL1; Flags: Precursorgi|45644965|sp|P25374.2|NFS1_YEASTProtein
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