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A DNA marker closely linked to the factor IX (haemophilia B) gene
A DNA marker closely linked to the factor IX (haemophilia B) gene
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A DNA marker closely linked to the factor IX (haemophilia B) gene

MULLIGAN, L ; HOLDEN, J. J. A ; WHITE, B. N

Human genetics, 1987-04, Vol.75 (4), p.381-383 [Periódico revisado por pares]

Heidelberg: Springer

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2
Cystic fibrosis: typing 48 German families with linked DNA probes
Cystic fibrosis: typing 48 German families with linked DNA probes
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Cystic fibrosis: typing 48 German families with linked DNA probes

MATHY, L ; KAMPMANN, W ; HIGUCHI, M ; SCHWARTENBECK, B ; BARTHOLOME, K ; DRIESEL, A. J ; GRZESCHIK, K.-H ; OLEK, K

Human genetics, 1987-04, Vol.75 (4), p.359-361 [Periódico revisado por pares]

Heidelberg: Springer

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3
Analysis of crossover type in the α-3.7 haplotype among sickle cell anemia patients from various parts of Africa
Analysis of crossover type in the α-3.7 haplotype among sickle cell anemia patients from various parts of Africa
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Analysis of crossover type in the α-3.7 haplotype among sickle cell anemia patients from various parts of Africa

DODE, C ; BERTH, A ; ROCHETTE, J ; GIROT, R ; LABIE, D

Human genetics, 1988-02, Vol.78 (2), p.193-195 [Periódico revisado por pares]

Heidelberg: Springer

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4
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis
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Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis

MORREAU, J ; SINAASAPPEL, M ; OOSTRA, B. A ; HALLEY, D. J. J

Human genetics, 1988-05, Vol.79 (1), p.64-67 [Periódico revisado por pares]

Heidelberg: Springer

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5
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II
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The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II

WESTPHAL, E.-M ; NATT, E ; GRIMM, T ; ODIEVRE, M ; SCHERER, G

Human genetics, 1988-07, Vol.79 (3), p.260-264 [Periódico revisado por pares]

Heidelberg: Springer

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6
DNA haplotype distribution in Algerian β thalassaemia patients: an extended evaluation by family studies and representative molecular characterization
DNA haplotype distribution in Algerian β thalassaemia patients: an extended evaluation by family studies and representative molecular characterization
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DNA haplotype distribution in Algerian β thalassaemia patients: an extended evaluation by family studies and representative molecular characterization

ROUABHI, F ; LAPOUMEROULIE, C ; AMSELEM, S ; KRISHNAMOORTHY, R ; ADJRAD, L ; GIROT, R ; CHARDIN, P ; BENABDJI, M ; LABIE, D ; BELDJORD, C

Human genetics, 1988-08, Vol.79 (4), p.373-376 [Periódico revisado por pares]

Heidelberg: Springer

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7
β-globin gene linked DNA haplotypes and frameworks in three South-East Asian populations
β-globin gene linked DNA haplotypes and frameworks in three South-East Asian populations
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β-globin gene linked DNA haplotypes and frameworks in three South-East Asian populations

HUNDRIESER, J ; SANGUANSERMSRI, T ; PAPP, T ; LAIG, M ; FLATZ, G

Human genetics, 1988-09, Vol.80 (1), p.90-94 [Periódico revisado por pares]

Heidelberg: Springer

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8
Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families
Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families
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Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families

KRAWCZAK, M ; KONECKI, D. S ; SCHMIDTKE, J ; DÜCK, M ; ENGEL, W ; NÜTZENADEL, W ; TREFZ, F. K

Human genetics, 1988-09, Vol.80 (1), p.78-80 [Periódico revisado por pares]

Heidelberg: Springer

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9
Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India
Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India
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Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India

Fodde, R ; Losekoot, M ; van den Broek, M H ; Oldenburg, M ; Rashida, N ; Schreuder, A ; Wijnen, J T ; Giordano, P C ; Nayudu, N V ; Khan, P M

Human genetics, 1988-10, Vol.80 (2), p.157-160 [Periódico revisado por pares]

Germany

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10
DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster
DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster
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DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster

ANTONARAKIS, S. E ; OETTGEN, P ; ARAVINDA CHAKRAVARTI ; HALLORAN, S. L ; HUDSON, R. R ; FEISEE, L ; KARATHANASIS, S. K

Human genetics, 1988-11, Vol.80 (3), p.265-273 [Periódico revisado por pares]

Heidelberg: Springer

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