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

Year Number of Results
1973 1
1975 3
1976 2
1977 1
1979 3
1981 2
1982 2
1983 1
1984 1
1985 4
1986 3
1987 4
1988 6
1989 3
1990 4
1991 2
1992 3
1993 5
1994 1
1996 1
1997 1
1998 1
1999 1
2003 1
2021 1
2022 1
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57 results
Results by year
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Page 1
Etiology and recurrence risk in Rubinstein-Taybi syndrome.
Hennekam RC, Stevens CA, Van de Kamp JJ. Hennekam RC, et al. Among authors: van de kamp jj. Am J Med Genet Suppl. 1990;6:56-64. doi: 10.1002/ajmg.1320370610. Am J Med Genet Suppl. 1990. PMID: 2118780 Review.
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.
Steele JL, Morrow MM, Sarnat HB, Alkhunaizi E, Brandt T, Chitayat DA, DeFilippo CP, Douglas GV, Dubbs HA, Elloumi HZ, Glassford MR, Hannibal MC, Héron B, Kim LE, Marco EJ, Mignot C, Monaghan KG, Myers KA, Parikh S, Quinonez SC, Rajabi F, Shankar SP, Shinawi MS, van de Kamp JJP, Veerapandiyan A, Waldman AT, Graf WD. Steele JL, et al. Among authors: van de kamp jjp. Pediatr Neurol. 2022 Jan;126:65-73. doi: 10.1016/j.pediatrneurol.2021.10.008. Epub 2021 Oct 18. Pediatr Neurol. 2022. PMID: 34740135 Free article.
Somatic origin of inherited haemophilia A.
Bröcker-Vriends AH, Briët E, Dreesen JC, Bakker B, Reitsma P, Pannekoek H, van de Kamp JJ, Pearson PL. Bröcker-Vriends AH, et al. Among authors: van de kamp jj. Hum Genet. 1990 Aug;85(3):288-92. doi: 10.1007/BF00206748. Hum Genet. 1990. PMID: 1975557
[Population genetics].
Fraser GR, van de Kamp JJ. Fraser GR, et al. Among authors: van de kamp jj. Ned Tijdschr Geneeskd. 1975 Sep 27;119(39):1502-6. Ned Tijdschr Geneeskd. 1975. PMID: 1178084 Dutch. No abstract available.
Monosomy 8p: an easily overlooked syndrome.
Bröcker-Vriends AH, Mooij PD, van Bel F, Beverstock GC, van de Kamp JJ. Bröcker-Vriends AH, et al. Among authors: van de kamp jj. J Med Genet. 1986 Apr;23(2):153-4. doi: 10.1136/jmg.23.2.153. J Med Genet. 1986. PMID: 3712390 Free PMC article.
57 results