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- [3] 2 HEREDITARY DEFECTS RELATED TO VITAMIN-D METABOLISM MAP TO THE SAME REGION OF HUMAN CHROMOSOME-12Q CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 1978 - 1978
- [4] NORMAL 24-HYDROXYLATION OF VITAMIN-D METABOLITES IN PATIENTS WITH VITAMIN-D-DEPENDENCY RICKETS TYPE-I - STRUCTURAL IMPLICATIONS FOR THE VITAMIN-D HYDROXYLASES JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (04): : 814 - 820
- [5] LINKAGE OF AUTOSOMAL DOMINANT TYPE-I HEREDITARY MOTOR AND SENSORY NEUROPATHY TO THE DUFFY LOCUS ON CHROMOSOME-1 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1982, 45 (08): : 669 - 674
- [6] LINKAGE OF AUTOSOMAL DOMINANT TYPE-I HEREDITARY MOTOR AND SENSORY NEUROPATHY (HMSN) TO THE DUFFY LOCUS ON CHROMOSOME-1 ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1983, 56 (01): : P18 - P19
- [7] EXCLUSION OF THE LOCUS FOR AUTOSOMAL RECESSIVE PSEUDOHYPOALDOSTERONISM TYPE-1 FROM THE MINERALOCORTICOID RECEPTOR GENE REGION ON HUMAN-CHROMOSOME 4Q BY LINKAGE ANALYSIS JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (11): : 3341 - 3345
- [9] CONFIRMATION OF THE LOCATION OF A WAARDENBURG SYNDROME TYPE-I MUTATION ON HUMAN-CHROMOSOME 2Q - TIGHT LINKAGE TO FN1 AND ALPP ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1991, 630 : 295 - 297
- [10] PROBABLE LOCATION OF USHER TYPE-I GENE ON CHROMOSOME-14Q BY LINKAGE WITH D14S13 (MLJ14 PROBE) CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 1988 - 1988