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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 1
1960 1
1962 1
1965 1
1967 1
1968 1
1975 1
1976 2
1979 1
1986 2
1989 1
1996 1
2024 0

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PubMed (OMIM) for id: 1163

14 results

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Page 1
CRANIOSYNOSTOSIS: A SURVEY OF 204 CASES.
ANDERSON FM, GEIGER L. ANDERSON FM, et al. J Neurosurg. 1965 Mar;22:229-40. doi: 10.3171/jns.1965.22.3.0229. J Neurosurg. 1965. PMID: 14306216 No abstract available.
The simulation of mendelism.
EDWARDS JH. EDWARDS JH. Acta Genet Stat Med. 1960;10:63-70. doi: 10.1159/000151119. Acta Genet Stat Med. 1960. PMID: 13725809 No abstract available.
Familial scaphocephaly in father and son.
MURPHY JW. MURPHY JW. U S Armed Forces Med J. 1953 Oct;4(10):1496-9. U S Armed Forces Med J. 1953. PMID: 13102753 No abstract available.
Genetic study of scaphocephaly.
Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. Am J Med Genet. 1996 Mar 29;62(3):282-5. doi: 10.1002/(SICI)1096-8628(19960329)62:3<282::AID-AJMG15>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8882788
Autosomal deletion mapping in man.
Nance WE, Engel E. Nance WE, et al. Science. 1967 Feb 10;155(3763):692-4. doi: 10.1126/science.155.3763.692. Science. 1967. PMID: 4959670
Chromosome 7 short arm deletion, 7p21----pter.
Schömig-Spingler M, Schmid M, Brosi W, Grimm T. Schömig-Spingler M, et al. Hum Genet. 1986 Nov;74(3):323-5. doi: 10.1007/BF00282559. Hum Genet. 1986. PMID: 3781561
14 results