scholarly article | Q13442814 |
P2093 | author name string | K Nakajima | |
K Baba | |||
Y Itakura | |||
K Hashizume | |||
A Sakurai | |||
M Katai | |||
P2860 | cites work | Isolation 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 tumors | Q24558744 | ||
Mutation and cancer: statistical study of retinoblastoma | Q24618185 | ||
A comprehensive genetic map of the human genome based on 5,264 microsatellites | Q27860812 | ||
Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1 | Q28257084 | ||
The 1993-94 Généthon human genetic linkage map | Q28288492 | ||
Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms | Q35601230 | ||
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland | Q35889219 | ||
Dinucleotide repeat polymorphism at the D11S534 locus | Q40505996 | ||
Multiple disease genes cause hypertrophic cardiomyopathy | Q40602713 | ||
The molecular genetics of the multiple endocrine neoplasia syndromes | Q40708313 | ||
Biology of polycystic kidney disease | Q40749706 | ||
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 0.95 | Q43721286 | ||
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 insulinoma | Q48100816 | ||
Candidate genes for multiple endocrine neoplasia type 1 | Q57423383 | ||
Multiple endocrine neoplasia type 1 (MEN1) in two Asian families | Q57423388 | ||
The importance of screening for the MEN 1 syndrome: diagnostic results and clinical management | Q67889196 | ||
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 1 | Q69369400 | ||
Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant | Q71739592 | ||
Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markers | Q71739620 | ||
Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndrome | Q71827858 | ||
Cause of death in multiple endocrine neoplasia type 1 | Q72220849 | ||
The influence of genetic counselling in the era of DNA testing on knowledge, reproductive intentions and psychological wellbeing | Q72407529 | ||
P433 | issue | 9 | |
P921 | main subject | founder effect | Q504568 |
multiple endocrine neoplasia | Q1553018 | ||
multiple endocrine neoplasia type 1 | Q3347154 | ||
P1104 | number of pages | 10 | |
P304 | page(s) | 985-994 | |
P577 | publication date | 1996-09-01 | |
P1433 | published in | Japanese Journal of Cancer Research | Q26842384 |
P1476 | title | Genetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families. | |
P478 | volume | 87 |
Q53914105 | Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1. |
Q34386474 | Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders |
Q55099861 | Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1. |
Q74626471 | Premature centromere division in patients with multiple endocrine neoplasia type 1 |
Q74791955 | Thymic carcinoids in multiple endocrine neoplasia type 1 |
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