Author:
Fiorentino F.,Biricik A.,Nuccitelli A.,De Palma R.,Kahraman S.,Iacobelli M.,Trengia V.,Caserta D.,Bonu M.A.,Borini A.,Baldi M.
Publisher
Oxford University Press (OUP)
Subject
Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine
Reference58 articles.
1. Boycott KM , Halley GR, Schlessinger D and Bech-Hansen NT (1996) A 2‐megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23–p11.22 from ZNF21 to DXS255. Genomics33,488–497.
2. Braude P , Pickering S, Flinter F and Ogilvie CM (2002) Preimplantation genetic diagnosis. Nat Rev Genet3,941–953.
3. Clemens PR , Fenwick RG, Chamberlain JS, Gibbs RA, de Andrade M, Chakraborty R and Caskey CT (1991) Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am J Hum Genet49,951–960.
4. Day DJ , Speiser PW, Schulze E, Bettendorf M, Fitness J, Barany F and White PC (1996) Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees. Hum Mol Genet5,2039–2048.
5. Dean NL , Tan SL and Ao A (2001) The development of preimplantation genetic diagnosis for myotonic dystrophy using multiplex fluorescent polymerase chain reaction and its clinical application. Mol Hum Reprod7,895–901.
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