-
1
-
-
0030035153
-
Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families
-
AN Akarsu I Stoilov E Yilmaz BS Sayli M Sarfarazi Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families Hum Mol Genet 5 1996 945 952
-
(1996)
Hum Mol Genet
, vol.5
, pp. 945-952
-
-
Akarsu, AN1
Stoilov, I2
Yilmaz, E3
Sayli, BS4
Sarfarazi, M5
-
4
-
-
0031127101
-
Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21
-
EA Bruford R Riise PW Teague K Porter KL Thomson AT Moore M Jay Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21 Genomics 41 1997 93 99
-
(1997)
Genomics
, vol.41
, pp. 93-99
-
-
Bruford, EA1
Riise, R2
Teague, PW3
Porter, K4
Thomson, KL5
Moore, AT6
Jay, M7
-
6
-
-
0024366485
-
High incidence of Bardet-Biedl syndrome among the Bedouin
-
TI Farag AS Teebi High incidence of Bardet-Biedl syndrome among the Bedouin Clin Genet 36 1989 463 465
-
(1989)
Clin Genet
, vol.36
, pp. 463-465
-
-
Farag, TI1
Teebi, AS2
-
7
-
-
0024472754
-
The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome
-
JS Green PS Parfrey JD Harnett NR Farid BC Cramer G Johnson O Heath The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome N Engl J Med 321 1989 1002 1009
-
(1989)
N Engl J Med
, vol.321
, pp. 1002-1009
-
-
Green, JS1
Parfrey, PS2
Harnett, JD3
Farid, NR4
Cramer, BC5
Johnson, G6
Heath, O7
-
8
-
-
0014605392
-
The syndrome of Lawrence-Moon-Bardet-Biedl and allied diseases in Switzerland
-
D Klein F Ammann The syndrome of Lawrence-Moon-Bardet-Biedl and allied diseases in Switzerland J Neurol Sci 9 1969 479 513
-
(1969)
J Neurol Sci
, vol.9
, pp. 479-513
-
-
Klein, D1
Ammann, F2
-
10
-
-
0023239442
-
Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children
-
ES Lander D Botstein Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children Science 236 1987 1567 1570
-
(1987)
Science
, vol.236
, pp. 1567-1570
-
-
Lander, ES1
Botstein, D2
-
12
-
-
0028000502
-
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping
-
VS Sheffield R Carmi A Kwitek-Black T Rokhlina D Nishimura GM Duyk K Elbedour Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping Hum Mol Genet 3 1994 1331 1335
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1331-1335
-
-
Sheffield, VS1
Carmi, R2
Kwitek-Black, A3
Rokhlina, T4
Nishimura, D5
Duyk, GM6
Elbedour, K7
-
13
-
-
0031790040
-
Use of isolated inbred human populations for identification of disease genes
-
VS Sheffield EM Stone R Carmi Use of isolated inbred human populations for identification of disease genes Trends Genet 14 1998 391 396
-
(1998)
Trends Genet
, vol.14
, pp. 391-396
-
-
Sheffield, VS1
Stone, EM2
Carmi, R3
-
15
-
-
0032963190
-
Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus
-
MO Woods TL Young PS Parfrey D Hefferton JS Green WS Davidson Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus Genomics 55 1999 2 9
-
(1999)
Genomics
, vol.55
, pp. 2-9
-
-
Woods, MO1
Young, TL2
Parfrey, PS3
Hefferton, D4
Green, JS5
Davidson, WS6
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