Genomic imprinting and its clinical implications. [N Engl J Med. 1992] - PubMed

Save items

loading

Related citations in PubMed

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15. [N Engl J Med. 1992]
Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.
Smeets DF, Hamel BC, Nelen MR, Smeets HJ, Bollen JH, Smits AP, Ropers HH, van Oost BA. N Engl J Med. 1992 Mar 19; 326(12):807-11.
Genomic imprinting in an Angelman and Prader-Willi translocation family. [Lancet. 1991]
Genomic imprinting in an Angelman and Prader-Willi translocation family.
Hultén M, Armstrong S, Challinor P, Gould C, Hardy G, Leedham P, Lee T, McKeown C. Lancet. 1991 Sep 7; 338(8767):638-9.
'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation. [Clin Genet. 2003]
'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation.
Matsumura M, Kubota T, Hidaka E, Wakui K, Kadowaki S, Ueta I, Shimizu T, Ueno I, Yamauchi K, Herzing LB, et al. Clin Genet. 2003 Jan; 63(1):79-81.
Review Prader-Willi syndrome and Robertsonian translocations involving chromosome 15. [Clin Genet. 1991]
Review Prader-Willi syndrome and Robertsonian translocations involving chromosome 15.
Casamassima AC, Shapiro LR, Wilmot PL, Smith KB. Clin Genet. 1991 Apr; 39(4):294-7.
Review Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models. [Acta Paediatr Suppl. 1999]
Review Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.
Nicholls RD, Ohta T, Gray TA. Acta Paediatr Suppl. 1999 Dec; 88(433):99-104.

See reviews... See all...

Cited by 3 PubMed Central articles

The role of mitochondrial haplogroups in primary open angle glaucoma. [Br J Ophthalmol. 2006]
The role of mitochondrial haplogroups in primary open angle glaucoma.
Andrews R, Ressiniotis T, Turnbull DM, Birch M, Keers S, Chinnery PF, Griffiths PG. Br J Ophthalmol. 2006 Apr; 90(4):488-90.
Review Mouse homologues of human hereditary disease. [J Med Genet. 1994]
Review Mouse homologues of human hereditary disease.
Searle AG, Edwards JH, Hall JG. J Med Genet. 1994 Jan; 31(1):1-19.
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1). [Am J Hum Genet. 1993]
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1).
Brandi ML, Weber G, Svensson A, Falchetti A, Tonelli F, Castello R, Furlani L, Scappaticci S, Fraccaro M, Larsson C. Am J Hum Genet. 1993 Dec; 53(6):1167-72.

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.

Recent activity

Clear Turn Off Turn On

Genomic imprinting and its clinical implications.
Genomic imprinting and its clinical implications.
N Engl J Med. 1992 Mar 19 ;326(12):827-9.

PubMed
The use, misuse and diversion of prescription stimulants among middle and high s...
The use, misuse and diversion of prescription stimulants among middle and high school students.
Subst Use Misuse. 2004 Jun ;39(7):1095-116.

PubMed
Cancer in the contralateral breast after radiotherapy for breast cancer.
Cancer in the contralateral breast after radiotherapy for breast cancer.
N Engl J Med. 1992 Mar 19 ;326(12):781-5.

PubMed
Caregiving for persons with mental illness: the impact of outpatient commitment ...
Caregiving for persons with mental illness: the impact of outpatient commitment on caregiving strain.
J Nerv Ment Dis. 2004 Aug ;192(8):554-62.

PubMed
Transplant ethics: altruism and materialism in organ donation.
Transplant ethics: altruism and materialism in organ donation.
Clin Transpl. 2003 :293-305.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to:

Genomic imprinting and its clinical implications.

Comment on

Publication Types, MeSH Terms

Publication Types

MeSH Terms

LinkOut - more resources

Full Text Sources

Medical

Supplemental Content

Save items

Related citations in PubMed

Cited by 3 PubMed Central articles

Related information

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information