Author:
Allanson J E,Upadhyaya M,Watson G H,Partington M,MacKenzie A,Lahey D,MacLeod H,Sarfarazi M,Broadhead W,Harper P S
Subject
Genetics (clinical),Genetics
Reference25 articles.
1. Pulmonary stenosis, cafe-au-lait spots, and dull intelligence;Watson, G.H.;Arch Dis Child,1967
2. Watson syndrome: nineteen years on;Allanson, J.E.; Watson, G.H.,1987
3. Pulmonary stenosis, cafe-au-lait spots and dull intelligence;Partington, M.W.; Burggraf, G.W.; Fay, J.E.; Frontini, E.
4. Noonan phenotype associated with neurofibromatosis;Allanson, J.E.; Hall, J.G.; Van Allen, M.I.;Am Med Genet,1985
5. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17;Barker, D.; Wright, E.C.; Nguyen, K.;Science,1987
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