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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 12p12.3 (Seller et al, 2006).
- Durkin S G, Glover T W.: Chromosome fragile sites. Ann. Rev. Genet. 41: 169-192, 2007. [PubMed: 17608616]
Glover T W, Stein C K: Chromosome breakage and recombination at fragile sites. AJHG 43:265-273, 1988. [PMC free article: PMC1715373] [PubMed: 3137811]Evidence was obtained to support the hypothesis that the fragile site represents a repeated sequence in studies of somatic cell hybrids in which breakages were induced by FUdR or aphidicolin at or close to Xq27 or 3p14.2.Aberration: Fragile sitesNegative band - Hashish A F, Monk N A, Watt A J, Gardner R J M: A de novo insertion, detected prenatally, with normal phenotype. J. Med. Genet. 29:351, 1992. [PMC free article: PMC1015960] [PubMed: 1583666]46,XX,dir ins(9;3)(q22.1;p14.2p25.1)de novo.Aberration: Direct insertion between two chromosomesNegative band
- Rassool F V, Le Beau M M, Shen M L, Neilly M E, Espinosa R III, Ong S T, Boldog F, Drabkin H, McCarroll R, McKeithan T W.: Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2. Genomics 35:109-117, 1996. [PubMed: 8661111]Aberration: Fragile sitesNegative band
- Tuerlings J H A M, de France H F, Hamers A, Hordijk R, Van Hemel J O, Hansson K, Hoovers J M N, Madan K, Van Der Blij-Philipsen M, Gerssen-Schoorl K B J, Kremer J A M, Smeets D F C M.: Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. Europ. J. Hum. Genet. 6:194-200, 1998. [PubMed: 9781022]46,XY,t(3;6)(p14.2;p25.1)Aberration: Simple translocationIndex Terms: ICSI
- 03p142 - Chromosomal Variation in Man03p142 - Chromosomal Variation in Man
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