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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1969 | 1 |
1995 | 1 |
2000 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 344290
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Genetic heterogeneity in Noonan syndrome: evidence for an autosomal recessive form.
Am J Med Genet. 2000 Sep 4;94(1):46-51. doi: 10.1002/1096-8628(20000904)94:1<46::aid-ajmg10>3.0.co;2-i.
Am J Med Genet. 2000.
PMID: 10982482
Isolation and characterization of a novel gene deleted in DiGeorge syndrome.
Kurahashi H, Akagi K, Inazawa J, Ohta T, Niikawa N, Kayatani F, Sano T, Okada S, Nishisho I.
Kurahashi H, et al.
Hum Mol Genet. 1995 Apr;4(4):541-9. doi: 10.1093/hmg/4.4.541.
Hum Mol Genet. 1995.
PMID: 7633402
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Familial Turner phenotype.
Abdel-Salam E, Temtamy SA.
Abdel-Salam E, et al.
J Pediatr. 1969 Jan;74(1):67-72. doi: 10.1016/s0022-3476(69)80009-0.
J Pediatr. 1969.
PMID: 5782826
No abstract available.
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