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| | 1 - 10 of 323 journal articles in the PubMed database | Email to a friend | | |
| Prasher VP, Krishnan VH, Clarke DJ, et al.
Deletion of chromosome 2 (p11-p13): case report and review. [Case Reports, Journal Article, Review]
J Med Genet 1993 Jul; 30(7):604-6.
Abstract | Full Citation | Find Related Articles | | Beall MH, Falk RE, Ying KL
A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4. [Case Reports, Journal Article, Review]
Am J Med Genet 1988 Nov; 31(3):553-7.
Abstract | Full Citation | Find Related Articles | | Kroes HY, Tuerlings JH, Hordijk R, et al.
Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32). [Journal Article, Review]
J Med Genet 1994 Feb; 31(2):156-8.
Abstract | Full Citation | Find Related Articles | | Stratton RF, Dobyns WB, Greenberg F, et al.
Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. [Case Reports, Journal Article]
Am J Med Genet 1986 Jul; 24(3):421-32.
Abstract | Full Citation | 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 | | Fischer H, Oswald HP, Duba HC, et al.
Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature. [Case Reports, Journal Article, Review]
Klin Padiatr 1993 May-Jun; 205(3):162-6.
Abstract | Full Citation | Find Related Articles | | Vogels A, de Smet L, van den Berghe H, et al.
Thrombocytopenia and cleft hand in monosomy 21. [Case Reports, Journal Article]
Genet Couns 1994; 5(1):67-71.
Abstract | Full Citation | Find Related Articles | | Grebe TA, Stevens MA, Byrne-Essif K, et al.
7p deletion syndrome: an adult with mild manifestations. [Journal Article, Research Support, Non-U.S. Gov't ]
Am J Med Genet 1992 Sep 1; 44(1):18-23.
Abstract | Full Citation | Find Related Articles | | Park JP, Moeschler JB, Berg SZ, et al.
A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant. [Case Reports, Journal Article]
Clin Genet 1992 Jan; 41(1):54-6.
Abstract | Full Citation | Find Related Articles |   |
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