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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1967 | 1 |
1991 | 1 |
1992 | 2 |
1993 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 107817
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Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome.
Am J Hum Genet. 1993 Jul;53(1):90-5.
Am J Hum Genet. 1993.
PMID: 8317503
Free PMC article.
Pulmonary stenosis, café-au-lait spots, and dull intelligence.
Watson GH.
Watson GH.
Arch Dis Child. 1967 Jun;42(223):303-7. doi: 10.1136/adc.42.223.303.
Arch Dis Child. 1967.
PMID: 6025371
Free PMC article.
No abstract available.
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Watson syndrome: is it a subtype of type 1 neurofibromatosis?
Allanson JE, Upadhyaya M, Watson GH, Partington M, MacKenzie A, Lahey D, MacLeod H, Sarfarazi M, Broadhead W, Harper PS, et al.
Allanson JE, et al.
J Med Genet. 1991 Nov;28(11):752-6. doi: 10.1136/jmg.28.11.752.
J Med Genet. 1991.
PMID: 1770531
Free PMC article.
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Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
Sharland M, Taylor R, Patton MA, Jeffery S.
Sharland M, et al.
J Med Genet. 1992 Mar;29(3):188-90. doi: 10.1136/jmg.29.3.188.
J Med Genet. 1992.
PMID: 1348095
Free PMC article.
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Analysis of mutations at the neurofibromatosis 1 (NF1) locus.
Upadhyaya M, Shen M, Cherryson A, Farnham J, Maynard J, Huson SM, Harper PS.
Upadhyaya M, et al.
Hum Mol Genet. 1992 Dec;1(9):735-40. doi: 10.1093/hmg/1.9.735.
Hum Mol Genet. 1992.
PMID: 1302608
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