TY - JOUR
T1 - Von Recklinghausen neurofibromatosis
T2 - A linkage study of candidate and random marker genes
AU - Ferrell, R. E.
AU - Buetow, K. H.
AU - Darby, J. K.
AU - Eichner, J. E.
AU - Murray, J. C.
AU - Smith, R.
AU - Waziri, M.
AU - Huson, S.
AU - Riccardi, V. M.
PY - 1987
Y1 - 1987
N2 - Genotyping, using plasma proteins or DNA polymorphisms or both, was carried out on 30 families selected through probands with Von Recklinghausen disease. The data provide additional evidence for the exclusion of loci on chromosomes 3 and 5, and chromosome arms 1q, 2p, 4p, 4q, 6q, 7p, 9q, 11p, 11q, and 14q. There was no evidence for genetic heterogeneity at D1S1 (DNF15S2) on chromosome arm 3p, using the Morton test for heterogeneity.
AB - Genotyping, using plasma proteins or DNA polymorphisms or both, was carried out on 30 families selected through probands with Von Recklinghausen disease. The data provide additional evidence for the exclusion of loci on chromosomes 3 and 5, and chromosome arms 1q, 2p, 4p, 4q, 6q, 7p, 9q, 11p, 11q, and 14q. There was no evidence for genetic heterogeneity at D1S1 (DNF15S2) on chromosome arm 3p, using the Morton test for heterogeneity.
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U2 - 10.1136/jmg.24.9.522
DO - 10.1136/jmg.24.9.522
M3 - Article
C2 - 3118028
AN - SCOPUS:0023270278
SN - 0022-2593
VL - 24
SP - 522
EP - 524
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
IS - 9
ER -