Gene mapping and neurogenetics.
P S Harper
J Med Genet 1987; 24: 513-514. doi:10.1136/jmg.24.9.513
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An exclusion map for Von Recklinghausen neurofibromatosis.
M Sarfarazi, S M Huson, and J H Edwards
J Med Genet 1987; 24: 515-520. doi:10.1136/jmg.24.9.515
[Abstract]
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Von Recklinghausen neurofibromatosis and genetic linkage studies: clinical considerations.
V M Riccardi and J C Carey
J Med Genet 1987; 24: 521-522. doi:10.1136/jmg.24.9.521
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Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.
R E Ferrell, K H Buetow, J K Darby, J E Eichner, J C Murray, R Smith, M Waziri, S Huson, and V M Riccardi
J Med Genet 1987; 24: 522-524. doi:10.1136/jmg.24.9.522
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Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis.
C G Mathew, K Thorpe, D F Easton, C Carter, C Wallis, Z Wong, A J Jeffreys, and B A Ponder
J Med Genet 1987; 24: 524-526. doi:10.1136/jmg.24.9.524
[Abstract]
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Linkage analysis of neurofibromatosis.
S Kittur, M L Lubs, M Bauer, A Chakravarti, and H Kazazian
J Med Genet 1987; 24: 526-527. doi:10.1136/jmg.24.9.526
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Genetic linkage studies with neurofibromatosis: the question of heterogeneity.
M A Spence, R S Sparkes, D M Parry, S J Bale, V Cortessis, and J J Mulvihill
J Med Genet 1987; 24: 527-529. doi:10.1136/jmg.24.9.527
[Abstract]
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DNA linkage analysis in Von Recklinghausen neurofibromatosis.
B R Seizinger, G Rouleau, A H Lane, L J Ozelius, A G Faryniarz, J Iannazzi, W Hobbs, J C Roy, B Falcone, and S Huson
J Med Genet 1987; 24: 529-530. doi:10.1136/jmg.24.9.529
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Linkage studies in peripheral neurofibromatosis.
M A Pericak-Vance, L H Yamaoka, J M Vance, A S Aylsworth, G O Rossenwasser, P C Gaskell, Jr, M J Alberts, W Y Hung, C Haynes, and A D Roses
J Med Genet 1987; 24: 530-532. doi:10.1136/jmg.24.9.530
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Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8.
S R Diehl, M Boehnke, F S Collins, R P Erickson, I J Karolyi, L M Ploughman, M A Pericak-Vance, A S Aylsworth, and A D Roses
J Med Genet 1987; 24: 532-534. doi:10.1136/jmg.24.9.532
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Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.
M Upadhyaya, M Sarfarazi, S M Huson, and P S Harper
J Med Genet 1987; 24: 534-536. doi:10.1136/jmg.24.9.534
[Abstract]
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A genomic search for linkage of neurofibromatosis to RFLPs.
D Barker, E Wright, K Nguyen, L Cannon, P Fain, D Goldgar, D T Bishop, J Carey, J Kivlin, and H Willard
J Med Genet 1987; 24: 536-538. doi:10.1136/jmg.24.9.536
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Exclusion mapping.
J H Edwards
J Med Genet 1987; 24: 539-543. doi:10.1136/jmg.24.9.539
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Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl.
J M Connor, L A Pirrit, J R Yates, A E Fryer, and M A Ferguson-Smith
J Med Genet 1987; 24: 544-546. doi:10.1136/jmg.24.9.544
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Tuberous sclerosis: a large family with no history of seizures or mental retardation.
A E Fryer, J P Osborne, R Tan, and D C Siggers
J Med Genet 1987; 24: 547-548. doi:10.1136/jmg.24.9.547
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The clinical spectrum of the Fraser syndrome: report of three new cases and review.
J Gattuso, M A Patton, and M Baraitser
J Med Genet 1987; 24: 549-555. doi:10.1136/jmg.24.9.549
[Abstract]
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Congenital cutis laxa with retardation of growth and development.
M A Patton, J Tolmie, P Ruthnum, S Bamforth, M Baraitser, and M Pembrey
J Med Genet 1987; 24: 556-561. doi:10.1136/jmg.24.9.556
[Abstract]
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Rubinstein-Taybi syndrome.
A C Berry
J Med Genet 1987; 24: 562-566. doi:10.1136/jmg.24.9.562
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Congenital non-chylous pleural effusion with Down's syndrome.
N Modi and R W Cooke
J Med Genet 1987; 24: 567-568. doi:10.1136/jmg.24.9.567
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Homozygosity in piebald trait.
M A Hultén, M M Honeyman, A J Mayne, and M J Tarlow
J Med Genet 1987; 24: 568-571. doi:10.1136/jmg.24.9.568
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