Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1.

Author:

Upadhyaya M,Fryer A,MacMillan J,Broadhead W,Huson S M,Harper P S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Neurofibromatosis: phenotype, natural history and pathogenesis;Riccardi, V.M.; Eichner, J.E.,1986

2. A genetic study of von Recklinghausen neurofibromatosis in south-east Wales. II. Guidelines for genetic counselling;Huson, S.M.; Compston, D.A.S.; Harper, P.S.;J Med Genet,1989

3. Gene for von Recklinghausen neurofibromatosis in the pericentromeric region of chromosome 17;Barker, D.; Wright, E.; Nguyen, K.;Science,1987

4. Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth receptor gene;Seizinger, B.R.; Rouleau, G.A.; Ozelius, L.J.;Cell,1987

5. Close flanking markers for neurofibromatosis type 1 (NFl);Upadhyaya, M.; Sarfarazi, M.; Huson, S.;Am J Hum Genet,1989

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2. Neurofibromatosis I;Atlas of Genetic Diagnosis and Counseling;2012

3. Neurofibromatosis 1: Analysis of the demand for prenatal diagnosis in a French cohort of 361 patients;American Journal of Medical Genetics Part A;2007

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