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1

Comments on important genetic topics from papers in other journals: Non-paternity and prenatal genetic screening

Comments on important genetic topics from papers in other journals: Non-paternity and prenatal genetic screening

Por Reardon, W
Publicado em 1992

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2

Medical genetics: advances in brief: Couple screening for cystic fibrosis

Medical genetics: advances in brief: Couple screening for cystic fibrosis

Por Reardon, W
Publicado em 1992

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3

Comments on important topics from papers in other journals: Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

Comments on important topics from papers in other journals: Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

Por Reardon, W
Publicado em 1992

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4

Comments on important genetic topics from papers in other journals: Association of nm23-H1 allelic deletions with distant metastases in colorectal carcinoma

Comments on important genetic topics from papers in other journals: Association of nm23-H1 allelic deletions with distant metastases in colorectal carcinoma

Por Reardon, W
Publicado em 1992

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5

Medical genetics: advances in brief: p53 germline mutations in Li-Fraumeni syndrome

Medical genetics: advances in brief: p53 germline mutations in Li-Fraumeni syndrome

Por Reardon, W
Publicado em 1992

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6

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

Por Reardon, W
Publicado em 1992

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7

Genetic deafness.

Genetic deafness.

Por Reardon, W
Publicado em 1992

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8

Medical genetics: advances in brief: Linkage of type 2 diabetes to the glucokinase gene

Medical genetics: advances in brief: Linkage of type 2 diabetes to the glucokinase gene

Por Reardon, W
Publicado em 1992

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9

Medical genetics: advances in brief: Deletions within chromosome 22q11 in familial congenital heart disease

Medical genetics: advances in brief: Deletions within chromosome 22q11 in familial congenital heart disease

Por Reardon, W
Publicado em 1993

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10

Medical genetics: advances in brief: Genetic susceptibility to multiple sclerosis linked to myelin basic protein

Medical genetics: advances in brief: Genetic susceptibility to multiple sclerosis linked to myelin basic protein

Por Reardon, W
Publicado em 1993

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11

Medical genetics: advances in brief

Medical genetics: advances in brief

Por Reardon, W
Publicado em 1993

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12

Medical genetics: advances in brief: Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

Medical genetics: advances in brief: Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

Por Reardon, W
Publicado em 1993

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13

Medical genetics: advances in brief: Congenital bilateral perisylvian syndrome: study of 31 patients

Medical genetics: advances in brief: Congenital bilateral perisylvian syndrome: study of 31 patients

Por Reardon, W
Publicado em 1993

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14

Medical genetics: advances in brief: Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene

Medical genetics: advances in brief: Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene

Por Reardon, W
Publicado em 1993

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15

Medical genetics: advances in brief: Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemia

Medical genetics: advances in brief: Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous fam...

Por Reardon, W
Publicado em 1993

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16

Medical genetics: advances in brief: Mitochondrial gene mutation in isletcell-antibody-positive patients who were initially non-insulin-dependent diabetics

Medical genetics: advances in brief: Mitochondrial gene mutation in isletcell-antibody-positive patients who were initially non-insulin-dependent diabetics

Por Reardon, W
Publicado em 1993

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17

Medical genetics: advances in brief

Medical genetics: advances in brief

Por Reardon, W
Publicado em 1994

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18

Sex linked deafness: Wilde revisited.

Sex linked deafness: Wilde revisited.

Por Reardon, W
Publicado em 1990

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19

Medical genetics: advances in brief

Medical genetics: advances in brief

Por Reardon, W
Publicado em 1994

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20

Medical genetics: advances in brief: Wolfram syndrome: a mitochondrial-mediated disorder?

Medical genetics: advances in brief: Wolfram syndrome: a mitochondrial-mediated disorder?

Por Reardon, W
Publicado em 1994

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