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

Year Number of Results
1967 2
1968 4
1969 1
1974 7
1976 3
1977 5
1978 2
1979 5
1980 7
1981 10
1982 3
1983 3
1984 5
1985 6
1986 7
1987 5
1988 2
1989 4
1990 2
1991 2
1992 4
1993 4
1994 7
1995 4
1996 5
1997 2
1998 1
1999 2
2006 2
2007 1
2021 0
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Similar articles for PMID: 3703649

116 results
Results by year
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Page 1
An unusual ocular finding associated with chromosome 1q deletion syndrome.
Wright LL, Schwartz MF, Schwartz S, Karesh J. Wright LL, et al. Pediatrics. 1986 May;77(5):786. Pediatrics. 1986. PMID: 3703649 No abstract available.
Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
Taysi K, Dengler DR, Jones LA, Heersma JR. Taysi K, et al. Ann Genet. 1981;24(4):245-7. Ann Genet. 1981. PMID: 7036843 Review. No abstract available.
Deletion of the distal long arm of chromosome 1: a definable syndrome.
Johnson VP, Heck LJ, Carter GA, Flom JO. Johnson VP, et al. Am J Med Genet. 1985 Dec;22(4):685-94. doi: 10.1002/ajmg.1320220405. Am J Med Genet. 1985. PMID: 4073121
Are 1q plus chromosomes harmless?
Gardner RJ, McCreanor HR, Parslow MI, Veale AM. Gardner RJ, et al. Clin Genet. 1974;6(5):383-93. Clin Genet. 1974. PMID: 4434654 No abstract available.
[The 4 p-syndrome].
Giuffre' L, Corso D, Cammarata M, Benigno V, Curcuru' M. Giuffre' L, et al. Pediatria (Napoli). 1977 Dec 31;85(4):589-604. Pediatria (Napoli). 1977. PMID: 613300 Italian. No abstract available.
[Wolf syndrome. Apropos of 2 cases].
García González P, Pedraz García C, Merino Marcos L, Salazar Veloz J, Escudero Bueno G, Salazar Villalobos V. García González P, et al. An Esp Pediatr. 1983 Feb;18(2):113-7. An Esp Pediatr. 1983. PMID: 6881733 Spanish.
Velocardiofacial syndrome (Shprintzen syndrome, chromosome 22q11 deletion syndrome).
Olney AH, Kolodziej P. Olney AH, et al. Ear Nose Throat J. 1998 Jun;77(6):460-1. Ear Nose Throat J. 1998. PMID: 9674319 Review. No abstract available.
Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
McDonald-McGinn DM, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Am J Med Genet. 1996 Aug 23;64(3):525-6. doi: 10.1002/ajmg.1320640304. Am J Med Genet. 1996. PMID: 8862635 No abstract available.
Neuroblastoma in patients with constitutional chromosomal changes.
Fryns JP. Fryns JP. Genet Couns. 1996;7(1):73. Genet Couns. 1996. PMID: 8652093 No abstract available.
Terminal deletion of the short arm of chromosome 3.
Lizcano-Gil LA, Figuera LE. Lizcano-Gil LA, et al. Genet Couns. 1994;5(1):35-8. Genet Couns. 1994. PMID: 8031533
116 results
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