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1

Comments on important genetic topics from papers in other journals: The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene i... mā Barber, John C K

I whakaputaina 1992

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2

Medical genetics: advances in brief: Diagnosis of genetic disease using recombinant DNA. Third edition mā Barber, John C K

I whakaputaina 1992

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3

Medical genetics: advances in brief: Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities mā Barber, John C K

I whakaputaina 1992

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4

Medical genetics: advances in brief: Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene mā Barber, John C K

I whakaputaina 1993

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5

Medical genetics: advances in brief mā Barber, John C K

I whakaputaina 1993

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6

Medical genetics: advances in brief: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumours mā Barber, John C K

I whakaputaina 1993

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7

Medical genetics: advances in brief: Identification of a second pseudo-autosomal region near the Xq and Yq telomeres mā Barber, John C K

I whakaputaina 1993

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8

Medical genetics: advances in brief: Complete characterization of a large marker chromosome by reverse and forward chromosome painting mā Barber, John C K

I whakaputaina 1993

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9

Medical genetics: advances in brief: Duplication in the hypoxanthine phosphoribosyl-transferase gene caused by Alu-Alu recombination in a patient with Lesch-Nyhan syndrome mā Barber, John C K

I whakaputaina 1993

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10

Medical genetics: advances in brief: Medical genetics: advances in brief mā Barber, John C K

I whakaputaina 1993

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11

Medical genetics: advances in brief: Identification of the von Hippel-Lindau disease tumour suppressor gene mā Barber, John C K

I whakaputaina 1993

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12

Medical genetics: advances in brief: Amyotrophic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase mā Barber, John C K

I whakaputaina 1993

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13

Medical genetics: advances in brief: Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci mā Barber, John C K

I whakaputaina 1994

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14

Medical genetics: advances in brief: Diagnosis of human genetic disease using recombinant DNA; fourth edition mā Barber, John C K

I whakaputaina 1994

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15

Medical genetics: advances in brief mā Barber, John C K

I whakaputaina 1994

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16

Medical genetics: advances in brief: SRVX, a sex reversing locus in Xp21.2→p22.11 mā Barber, John C K

I whakaputaina 1994

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17

Medical genetics: advances in brief mā Barber, John C K

I whakaputaina 1994

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18

Medical genetics: advances in brief: Localization of the achondroplasia gene to the distal 2-5 Mb of human chromosome 4p mā Barber, John C K

I whakaputaina 1994

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19

Medical genetics: advances in brief mā Barber, John C K

I whakaputaina 1995

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20

Medical genetics: advances in brief: Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation mā Barber, John C K

I whakaputaina 1995

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Ngā hua rapu - Barber, John C. K.

Comments on important genetic topics from papers in other journals: The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene i... mā Barber, John C K

Medical genetics: advances in brief: Diagnosis of genetic disease using recombinant DNA. Third edition mā Barber, John C K

Medical genetics: advances in brief: Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities mā Barber, John C K

Medical genetics: advances in brief: Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene mā Barber, John C K

Medical genetics: advances in brief mā Barber, John C K

Medical genetics: advances in brief: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumours mā Barber, John C K

Medical genetics: advances in brief: Identification of a second pseudo-autosomal region near the Xq and Yq telomeres mā Barber, John C K

Medical genetics: advances in brief: Complete characterization of a large marker chromosome by reverse and forward chromosome painting mā Barber, John C K

Medical genetics: advances in brief: Duplication in the hypoxanthine phosphoribosyl-transferase gene caused by Alu-Alu recombination in a patient with Lesch-Nyhan syndrome mā Barber, John C K

Medical genetics: advances in brief: Medical genetics: advances in brief mā Barber, John C K

Medical genetics: advances in brief: Identification of the von Hippel-Lindau disease tumour suppressor gene mā Barber, John C K

Medical genetics: advances in brief: Amyotrophic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase mā Barber, John C K

Medical genetics: advances in brief: Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci mā Barber, John C K

Medical genetics: advances in brief: Diagnosis of human genetic disease using recombinant DNA; fourth edition mā Barber, John C K

Medical genetics: advances in brief mā Barber, John C K

Medical genetics: advances in brief: SRVX, a sex reversing locus in Xp21.2→p22.11 mā Barber, John C K

Medical genetics: advances in brief mā Barber, John C K

Medical genetics: advances in brief: Localization of the achondroplasia gene to the distal 2-5 Mb of human chromosome 4p mā Barber, John C K

Medical genetics: advances in brief mā Barber, John C K

Medical genetics: advances in brief: Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation mā Barber, John C K

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