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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1979 | 1 |
1990 | 1 |
1997 | 2 |
1998 | 1 |
1999 | 1 |
2000 | 1 |
2023 | 0 |
PubMed (OMIM) for id: 96605
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Page 1
The spectrum of growth abnormalities in children with 18q deletions.
J Clin Endocrinol Metab. 2000 Dec;85(12):4450-4. doi: 10.1210/jcem.85.12.7016.
J Clin Endocrinol Metab. 2000.
PMID: 11134092
Clinical Trial.
An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA.
Katz SG, Schneider SS, Bartuski A, Trask BJ, Massa H, Overhauser J, Lalande M, Lansdorp PM, Silverman GA.
Katz SG, et al.
Hum Mol Genet. 1999 Jan;8(1):87-92. doi: 10.1093/hmg/8.1.87.
Hum Mol Genet. 1999.
PMID: 9887335
Item in Clipboard
Identification of cryptic rearrangements in patients with 18q- deletion syndrome.
Brkanac Z, Cody JD, Leach RJ, DuPont BR.
Brkanac Z, et al.
Am J Hum Genet. 1998 Jun;62(6):1500-6. doi: 10.1086/301854.
Am J Hum Genet. 1998.
PMID: 9585582
Free PMC article.
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Growth hormone insufficiency associated with haploinsufficiency at 18q23.
Cody JD, Hale DE, Brkanac Z, Kaye CI, Leach RJ.
Cody JD, et al.
Am J Med Genet. 1997 Sep 5;71(4):420-5.
Am J Med Genet. 1997.
PMID: 9286448
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Growth hormone deficiency associated in the 18q deletion syndrome.
Ghidoni PD, Hale DE, Cody JD, Gay CT, Thompson NM, McClure EB, Danney MM, Leach RJ, Kaye CI.
Ghidoni PD, et al.
Am J Med Genet. 1997 Mar 3;69(1):7-12. doi: 10.1002/(sici)1096-8628(19970303)69:1<7::aid-ajmg2>3.0.co;2-p.
Am J Med Genet. 1997.
PMID: 9066876
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Growth hormone deficiency in children with chromosomal abnormalities.
Schwarz HP, Duck SC.
Schwarz HP, et al.
Arch Dis Child. 1990 Mar;65(3):334. doi: 10.1136/adc.65.3.334-a.
Arch Dis Child. 1990.
PMID: 2378627
Free PMC article.
No abstract available.
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Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
Wilson MG, Towner JW, Forsman I, Siris E.
Wilson MG, et al.
Am J Med Genet. 1979;3(2):155-74. doi: 10.1002/ajmg.1320030207.
Am J Med Genet. 1979.
PMID: 474629
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