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TY  - GEN
AU  - McKusick, V.A.
TI  - Mendelian Inheritance in Man
PY  - 1992///
ER  - 

TY  - JOUR
AU  - Marmor, M.F.
TI  - Retinitis pigmentosa: A symposium on terminology and methods of examination
JO  - Ophthalmology.
PY  - 1983///
VL  - 90
SP  - 126
EP  - 131
ER  - 

TY  - JOUR
AU  - Horing
TI  - Retinitis pigmentosa
JO  - Klin. monatsbl. Augenheilk.
PY  - 1864///
VL  - 2
SP  - 233
EP  - 235
ER  - 

TY  - JOUR
AU  - Wecker, L.
TI  - Annotations concernant le travail Hoering
JO  - Ann. Ocul.
PY  - 1865///
VL  - 53
SP  - 73
EP  - 73
ER  - 

TY  - GEN
AU  - Bardet, G.
TI  - Sur un syndrome d'obesite infantile avec polydactylie et retinite pigmentaire
PY  - 1920///
ER  - 

TY  - JOUR
AU  - Biedl, A.
TI  - Ein Geschwisterpaar mit adiposogenitaler dystrophie
JO  - Dtsch. med. Wochenschr.
PY  - 1922///
VL  - 48
SP  - 1630
EP  - 1630
ER  - 

TY  - JOUR
AU  - Raab, W.
TI  - Klinische und rontgenologische Beitrage zur hypophysaren zerebralen. Fettsucht und Genitalatrophie
JO  - Wien. Arch. inn. Med.
PY  - 1924///
VL  - 7
SP  - 443
EP  - 530
ER  - 

TY  - JOUR
AU  - Radner, S.
TI  - On Laurence-Moon-Biedl's syndrome
JO  - Acta med. Scand.
PY  - 1940///
VL  - 105
SP  - 141
EP  - 152
ER  - 

TY  - JOUR
AU  - Landau, J.
AU  - Bromberg, Y.M.
AU  - Schorr, J.
TI  - Laurence-Moon-Biedl syndrome with multiple congenital malformations of the urinary tract
JO  - Acta med. Orient.
PY  - 1949///
VL  - 8
SP  - 205
EP  - 210
ER  - 

TY  - JOUR
AU  - Fraccaro, M.
AU  - Gastaldi, F.
TI  - La patologia della sindrome di Laurence-Moon-Biedl
JO  - Folia hered. Pathol.
PY  - 1953///
VL  - 2
SP  - 177
EP  - 214
ER  - 

TY  - JOUR
AU  - Ross, D.F.
AU  - Crome, L.
AU  - MacKenzie, D.Y.
TI  - The Laurence-Moon-Biedl syndrome
JO  - J. Pathol. Bacteriol.
PY  - 1956///
VL  - 72
SP  - 161
EP  - 172
ER  - 

TY  - JOUR
AU  - Klein, D.
AU  - Ammann, F.
TI  - The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland: clinical, genetic and epidemiologic studies
JO  - J. neurol. Sci.
PY  - 1969///
VL  - 9
SP  - 479
EP  - 513
M3  - 10.1016/0022-510X(69)90091-4
N1  - 10.1016/0022-510X(69)90091-4
UR  - http://dx.doi.org/10.1016/0022-510X(69)90091-4
ER  - 

TY  - GEN
AU  - Bell, J.
TI  - The Treasury of Human Inheritance
PY  - 1958///
VL  - 5
ER  - 

TY  - JOUR
AU  - Burn, R.A.
TI  - Deafness and the Laurence-Moon-Biedl syndrome
JO  - Br. J. Ophthalmol.
PY  - 1950///
VL  - 34
SP  - 65
EP  - 88
ER  - 

TY  - JOUR
AU  - Bauman, M.L.
AU  - Hogan, G.R.
TI  - Laurence-Moon-Biedl syndrome: Report of two unrelated children less than 3 years of age
JO  - Am. J. Dis. Child.
PY  - 1973///
VL  - 126
SP  - 119
EP  - 126
ER  - 

TY  - JOUR
AU  - Laurence, J.Z.
AU  - Moon, R.C.
TI  - Four cases of [ldquo]retinitis pigmentosa,[rdquo] occurring in the same family, and accompanied by general imperfections of development
JO  - Ophthal. Rev.
PY  - 1866///
VL  - 2
SP  - 32
EP  - 41
ER  - 

TY  - JOUR
AU  - Hutchinson, J.
TI  - On retinitis pigmentosa and allied affections, as illustrating the laws of heredity
JO  - Ophthal. Rev.
PY  - 1882///
VL  - 1
SP  - 26
EP  - 30
ER  - 

TY  - JOUR
AU  - Hutchinson, J.
TI  - Slowly progressive paraplegia and disease of the choroids, with defective intellect and arrested sexual development in several brothers and a sister
JO  - Arch. Surg.
PY  - 1900///
VL  - 11
SP  - 118
EP  - 122
ER  - 

TY  - JOUR
AU  - Kapuscinski, W.
TI  - Uber familiare Aderhautentartung mit ataktischen Storungen
JO  - Ber. Dtsch. Ophthalmol. Ges.
PY  - 1934///
VL  - 50
SP  - 13
EP  - 19
ER  - 

TY  - JOUR
AU  - Green, J.S.
TI  - The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome
JO  - New Engl. J. Med.
PY  - 1989///
VL  - 321
SP  - 1002
EP  - 1009
ER  - 

TY  - JOUR
AU  - Ammann, F.
TI  - Investigations cliniques et genetiques sur le syndrome de Bardet-Biedl en Suisse
JO  - J. Genet. Hum.
PY  - 1970///
VL  - 18
SP  - 1
EP  - 310
ER  - 

TY  - JOUR
AU  - Dekaban, A.S.
AU  - Parks, J.S.
AU  - Ross, G.T.
TI  - Laurence-Moon syndrome: evaluation of endocrinological function and phenotypic concordance and report of cases
JO  - Med. Ann. D. C.
PY  - 1972///
VL  - 41
SP  - 687
EP  - 694
ER  - 

TY  - JOUR
AU  - Cockayne, E.A.
AU  - Krestin, D.
AU  - Sorsby, A.
TI  - Obesity, hypogenitalism, mental retardation, polydactyly, and retinal pigmentation: the Laurence-Moon-Biedl syndrome
JO  - Quart. J. Med.
PY  - 1935///
VL  - 4
SP  - 93
EP  - 120
ER  - 

TY  - JOUR
AU  - Sorsby, A.
AU  - Avery, H.
AU  - Cockayne, E.A.
TI  - Obesity, hypogenitalism, mental retardation, polydactyly, and retinal pigmentation: the Laurence-Moon-Biedl syndrome
JO  - Quart. J. Med.
PY  - 1939///
VL  - 8
SP  - 51
EP  - 68
ER  - 

TY  - JOUR
AU  - Bergsma, D.R.
AU  - Brown, K.S.
TI  - Assessment of ophthalmologic, endocrinologic and genetic findings in the Bardet-Biedl syndrome
JO  - Birth Detects: Orig. Art. Ser.
PY  - 1975///
VL  - 11
SP  - 132
EP  - 136
ER  - 

TY  - JOUR
AU  - Kwitek-Black, A.E.
TI  - Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity
JO  - Nature Genet.
PY  - 1993///
VL  - 5
SP  - 392
EP  - 396
M3  - 10.1038/ng1293-392
N1  - 10.1038/ng1293-392
UR  - http://dx.doi.org/10.1038/ng1293-392
ER  - 

TY  - JOUR
AU  - Stone, E.M.
AU  - Nichols, B.E.
AU  - Streb, L.M.
AU  - Kimura, A.E.
AU  - Sheffield, V.C.
TI  - Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
JO  - Nature Genet.
PY  - 1992///
VL  - 1
SP  - 246
EP  - 250
M3  - 10.1038/ng0792-246
N1  - 10.1038/ng0792-246
UR  - http://dx.doi.org/10.1038/ng0792-246
ER  - 

TY  - JOUR
AU  - Bascom, R.A.
TI  - Cloning of the cDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies
JO  - Neurons
PY  - 1992///
VL  - 8
SP  - 1171
EP  - 1184
ER  - 

TY  - GEN
AU  - Stevenson, R.E.
AU  - Hall, J.G.
AU  - Goodman, R.M.
TI  - Human Malformation and Related Anomalies
PY  - 1993///
VL  - 2
ER  - 

TY  - JOUR
AU  - Lewis, R.A.
AU  - Otterud, B.
AU  - Stauffer, D.
AU  - Lalouel, J.-M.
AU  - Leppert, M.
TI  - Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q
JO  - Genomics
PY  - 1990///
VL  - 7
SP  - 250
EP  - 256
ER  - 

TY  - JOUR
AU  - Iwasaki, H.
TI  - A minisatellite and a mlnisatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0. 95
JO  - Genomics
PY  - 1992///
VL  - 13
SP  - 7
EP  - 15
ER  - 

TY  - JOUR
AU  - Polymeropoulos, M.H.
AU  - Xiao, H.
AU  - Rath, D.S.
AU  - Merril, C.R.
TI  - Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2)
JO  - Nucl. Acids Res.
PY  - 1990///
VL  - 18
SP  - 7468
EP  - 7468
ER  - 

TY  - JOUR
AU  - Weissenbach, J.
TI  - A second-generation linkage map of the human genome
JO  - Nature
PY  - 1992///
VL  - 359
SP  - 794
EP  - 801
M3  - 10.1038/359794a0
N1  - 10.1038/359794a0
UR  - http://dx.doi.org/10.1038/359794a0
ER  - 

TY  - JOUR
TI  - A comprehensive genetic linkage map of the human genome
JO  - Science
PY  - 1992///
VL  - 258
SP  - 67
EP  - 86
ER  - 

TY  - JOUR
AU  - Lathrop, G.M.
AU  - Lalouel, J.-M.
AU  - Julier, C.
AU  - Ott, J.
TI  - Multilocus linkage analysis in humans: detection of linkage and estimation of recombination
JO  - Am. J. hum. Genet.
PY  - 1985///
VL  - 37
SP  - 482
EP  - 498
ER  - 

TY  - JOUR
AU  - Ott, J.
TI  - Linkage analysis and family classification under heterogeneity
JO  - Ann. hum. Genet.
PY  - 1983///
VL  - 47
SP  - 311
EP  - 320
ER  - 

