Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia

Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17

1987 • 691 citations

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

1985 • 456 citations

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

1987 • 379 citations

Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.

1989 • 137 citations

The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105–q21.05

1989 • 57 citations

Genetic analysis of NF1: Identification of close flanking markers on chromosome 17

1987 • 55 citations

The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus.

1989 • 47 citations

Tightly linked markers for the neurofibromatosis type 1 gene

1987 • 39 citations

Refined physical and genetic mapping of the NF1 region on chromosome 17.

1989 • 35 citations

Genetic analysis of eight loci tightly linked to neurofibromatosis 1.

1989 • 14 citations

The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17

1990 • 7 citations

Mspl RFLP at CRYB1 locus (17q11.2 – 17q12)

1989 • 4 citations

XYY Genotype

1975 • 1 citations

Molecular Lesions Induced by I-R Hybrid Dysgenesis in Drosophila melanogaster

1989 • 1 citations