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| Ramer JC, Ladda RL, Frankel CA, et al.
A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2. [Case Reports, Journal Article, Review]
Am J Med Genet 1989 Mar; 32(3):359-63.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Gorski JL, Cox BA, Kyine M, et al.
Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37). [Case Reports, Journal Article]
Am J Med Genet 1989 Mar; 32(3):350-2.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Courtens W, Speleman F, Messiaen L, et al.
Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome. [Case Reports, Journal Article, Review]
Am J Med Genet 1997 Sep 5; 71(4):479-85.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Garcia-Miñaur S, Ramsay J, Grace E, et al.
Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3. [Case Reports, Journal Article, Review]
Am J Med Genet A 2005 Feb 1; 132(4):402-10.
Abstract | Full Citation | Find Related Articles | | Conrad B, Dewald G, Christensen E, et al.
Clinical phenotype associated with terminal 2q37 deletion. [Case Reports, Journal Article, Review]
Clin Genet 1995 Sep; 48(3):134-9.
Abstract | Full Citation | Find Related Articles | | Mackie Ogilvie C, Rooney SC, Hodgson SV, et al.
Deletion of chromosome 3q proximal region gives rise to a variable phenotype. [Case Reports, Journal Article]
Clin Genet 1998 Mar; 53(3):220-2.
Abstract | Full Citation | Find Related Articles | | Stockton DW, Ross HL, Bacino CA, et al.
Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review. [Case Reports, Journal Article]
Am J Med Genet 1997 Aug 8; 71(2):189-93.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Benson K, Gordon M, Wassman ER, et al.
Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33). [Case Reports, Journal Article]
Am J Med Genet 1986 Nov; 25(3):405-11.
Abstract | Full Citation | Find Related Articles | | Casas KA, Mononen TK, Mikail CN, et al.
Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals. [Case Reports, Journal Article]
Am J Med Genet A 2004 Nov 1; 130(4):331-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
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