Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus.
Familial multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant disorder characterized by the combined occurrence of tumors of the parathyroid glands, the endocrine pancreas, and the pituitary gland. MEN 1 tumors have previously been shown to be associated with the loss of alleles on c...
Prif Awduron: | Pang, J, Pook, M, Eubanks, J, Jones, C, van Heyningen, V, Evans, G, Thakker, R |
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Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
1992
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Eitemau Tebyg
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The molecular genetics of the multiple endocrine neoplasia syndromes.
gan: Thakker, R
Cyhoeddwyd: (1993) -
Molecular genetics and patient management of multiple endocrine neoplasia type I
gan: Thakker, R
Cyhoeddwyd: (2001) -
The role of molecular genetics in screening for multiple endocrine neoplasia type 1.
gan: Thakker, R
Cyhoeddwyd: (1994) -
Multiple endocrine neoplasia type 1 (MEN1).
gan: Pang, J, et al.
Cyhoeddwyd: (1994) -
MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
gan: Pang, J, et al.
Cyhoeddwyd: (1993)