Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK

References

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	Year	Citations
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member J. David Brook, Mila E. McCurrach, H G Harley, Cell Signal TransductionMendelian DisorderGenetic DisorderMedicineGenetics	1992	2.8K
ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011 Martine De Rycke, Florence Belva, V. Goossens, Human Reproduction	2015	707
Birth of a Normal Girl after in Vitro Fertilization and Preimplantation Diagnostic Testing for Cystic Fibrosis Alan H. Handyside, J G Lesko, Juan J. Tarı́n, New England Journal of Medicine	1992	543
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma. Paola Amicucci, Massimo Gennarelli, Giuseppe Novelli, PubMed Genetic TestingDm Kinase GeneGeneticsGenetic EpidemiologyFetal Medicine	2000	206
Prenatal Diagnosis of Myotonic Dystrophy Using Fetal DNA Obtained from Maternal Plasma Paola Amicucci, Massimo Gennarelli, Giuseppe Novelli, Clinical Chemistry Fetal MedicineGynecologyMaternal HealthPrenatal DiagnosisMaternal-fetal Medicine	2000	205
Genetic testing of embryos: practices and perspectives of US in vitro fertilization clinics Susannah Baruch, David Kaufman, Kathy Hudson Fertility and Sterility Genetic TestingFertilityGeneticsReproductive HealthGynecology	2007	154
ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004 Karen Sermon, A. Michiels, G. Harton, Human Reproduction	2006	107
Strategies for preimplantation genetic diagnosis of single gene disorders by DNA amplification Dagan Wells, Jon Sherlock Prenatal Diagnosis Genetic TestingGeneticsDna AnalysisMolecular BiologyPreimplantation Genetic Testing	1998	101
PGD in the lab for triplet repeat diseases ? myotonic dystrophy, Huntington's disease and Fragile-X syndrome Karen Sermon Molecular and Cellular Endocrinology Triplet Repeat DiseasesMendelian DisorderGenetic DisorderMedicineGenetics	2001	83
Characterization and Polymerase Chain Reaction (PCR) Detection of an Alu Deletion Polymorphism in Total Linkage Disequilibrium with Myotonic Dystrophy Mani S. Mahadevan, Martha A. Foitzik, Linda Surh, Genomics Polymerase Chain ReactionAlu Deletion PolymorphismMendelian DisorderGenetic DisorderMedicine	1993	53

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