| scholarly article | Q13442814 |
| P50 | author | Christopher G. Mathew | Q30348903 |
| P2093 | author name string | B A Ponder | |
| H Telenius | |||
| C Schuemichen | |||
| W Schempp | |||
| H P Neumann | |||
| N Freudenberg | |||
| P Schollmeyer | |||
| O A Müller | |||
| P2860 | cites work | Genomic sequencing | Q24594942 |
| "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 | ||
| Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred | Q33671201 | ||
| High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndrome | Q33862888 | ||
| Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants | Q35013854 | ||
| Bovine interstitial retinol-binding protein (IRBP)--isolation and sequence analysis of cDNA clones, characterization and in vitro translation of mRNA. | Q36469149 | ||
| Blot hybridisation analysis of genomic DNA | Q40076874 | ||
| Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 [D10S15] | Q40536609 | ||
| A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 | Q55670968 | ||
| Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage | Q57319205 | ||
| Sipple's syndrome: medullary thyroid carcinoma, pheochromocytoma, and parathyroid disease. Studies in a large family. NIH conference | Q69383028 | ||
| Absence of chromosomal instability in one kindred with multiple endocrine neoplasia type 2A | Q69881570 | ||
| Characteristics of a family with the MEN-2A syndrome | Q69910439 | ||
| Multiple endocrine neoplasia type 2A: a Northern Ireland and Australian family | Q69910441 | ||
| Screening multiple endocrine neoplasia type 2A families using DNA markers | Q69910837 | ||
| Risk estimation and screening in families of patients with medullary thyroid carcinoma | Q69912692 | ||
| The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience | Q69912831 | ||
| Identification of human chromosomes by DNA-binding fluorescent agents | Q70137712 | ||
| Cytologic evidence for three human X-chromosomal segments escaping inactivation | Q71229923 | ||
| P433 | issue | 18 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | multiple endocrine neoplasia | Q1553018 |
| diagnosis | Q16644043 | ||
| P304 | page(s) | 951-6 | |
| P577 | publication date | 1989-09-15 | |
| P1433 | published in | Klinische Wochenschrift | Q27711855 |
| P1476 | title | Early diagnosis of multiple endocrine neoplasia type IIa | |
| P478 | volume | 67 |
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