Genetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families.

scientific article published in September 1996

Genetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1349-7006.1996.TB02130.X
P932PMC publication ID5921204
P698PubMed publication ID8878463
P5875ResearchGate publication ID14327366

P2093author name stringK Nakajima
K Baba
Y Itakura
K Hashizume
A Sakurai
M Katai
P2860cites workIsolation and characterization of a novel gene encoding nuclear protein at a locus (D11S636) tightly linked to multiple endocrine neoplasia type 1 (MEN1)Q24319691
Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumorsQ24558744
Mutation and cancer: statistical study of retinoblastomaQ24618185
A comprehensive genetic map of the human genome based on 5,264 microsatellitesQ27860812
Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1Q28257084
The 1993-94 Généthon human genetic linkage mapQ28288492
Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphismsQ35601230
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from NewfoundlandQ35889219
Dinucleotide repeat polymorphism at the D11S534 locusQ40505996
Multiple disease genes cause hypertrophic cardiomyopathyQ40602713
The molecular genetics of the multiple endocrine neoplasia syndromesQ40708313
Biology of polycystic kidney diseaseQ40749706
Prospective screening in multiple endocrine neoplasia type 1.Q42453717
A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95Q43721286
Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.Q45094261
Should we test children for "adult" genetic diseases?Q45293856
Allele loss on chromosome 11 in a pituitary tumor from a patient with multiple endocrine neoplasia type 1.Q46892946
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinomaQ48100816
Candidate genes for multiple endocrine neoplasia type 1Q57423383
Multiple endocrine neoplasia type 1 (MEN1) in two Asian familiesQ57423388
The importance of screening for the MEN 1 syndrome: diagnostic results and clinical managementQ67889196
The natural history of multiple endocrine neoplasia type 1. Highly uncommon or highly unrecognized?Q68309763
Loss of the same alleles of HRAS1 and D11S151 in two independent pancreatic cancers from a patient with multiple endocrine neoplasia type 1Q69369400
Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinantQ71739592
Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markersQ71739620
Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndromeQ71827858
Cause of death in multiple endocrine neoplasia type 1Q72220849
The influence of genetic counselling in the era of DNA testing on knowledge, reproductive intentions and psychological wellbeingQ72407529
P433issue9
P921main subjectfounder effectQ504568
multiple endocrine neoplasiaQ1553018
multiple endocrine neoplasia type 1Q3347154
P1104number of pages10
P304page(s)985-994
P577publication date1996-09-01
P1433published inJapanese Journal of Cancer ResearchQ26842384
P1476titleGenetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families.
P478volume87

Reverse relations

cites work (P2860)
Q53914105Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.
Q34386474Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders
Q55099861Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1.
Q74626471Premature centromere division in patients with multiple endocrine neoplasia type 1
Q74791955Thymic carcinoids in multiple endocrine neoplasia type 1

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