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Results 1 - 20 of 801  for All Library Resources

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1
DELAYED ONTOGENESIS IN HUMAN TRISOMY SYNDROMES
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Article
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DELAYED ONTOGENESIS IN HUMAN TRISOMY SYNDROMES

Hereditas, 1965-01, Vol.52 (3), p.334-344 [Peer Reviewed Journal]

ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1965.tb01966.x ;PMID: 4220490

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2
PARTIAL MONOSOMY OF THE LONG ARM OF AN E CHROMOSOME - A NEW SYNDROME
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Article
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PARTIAL MONOSOMY OF THE LONG ARM OF AN E CHROMOSOME - A NEW SYNDROME

Hereditas, 1967-01, Vol.57 (1-2), p.205-208 [Peer Reviewed Journal]

1967 Hereditas ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1967.tb02102.x ;PMID: 6080797

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3
Twinning and associated stillbirth in Sweden, 1871-1960
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Article
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Twinning and associated stillbirth in Sweden, 1871-1960

Hereditas, 1970-01, Vol.64 (2), p.193-198 [Peer Reviewed Journal]

1970 Hereditas ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1970.tb02290.x ;PMID: 5535787

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4
Pericentric inversion Y in a population of newborn boys
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Article
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Pericentric inversion Y in a population of newborn boys

Hereditas, 1974, Vol.76 (1), p.147-152 [Peer Reviewed Journal]

ISSN: 0018-0661 ;EISSN: 1601-5223 ;PMID: 4136008

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5
A case of trisomy-G with a simultaneous balanced D-D translocation
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Article
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A case of trisomy-G with a simultaneous balanced D-D translocation

Hereditas, 1974-01, Vol.77 (1), p.159-162 [Peer Reviewed Journal]

1974 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1974.tb01359.x ;PMID: 4277975

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6
Stable Mycoplasma Antigen Preparations for Indirect Hemagglutination Tests
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Article
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Stable Mycoplasma Antigen Preparations for Indirect Hemagglutination Tests

Applied Microbiology, 1974-02, Vol.27 (2), p.356-359 [Peer Reviewed Journal]

Copyright © 1974 American Society for Microbiology ;ISSN: 0099-2240 ;ISSN: 0003-6919 ;EISSN: 1098-5336 ;DOI: 10.1128/AEM.27.2.356-359.1974 ;PMID: 4207279

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7
Extra marker chromosome in newborn children
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Article
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Extra marker chromosome in newborn children

Hereditas, 1975-01, Vol.81 (2), p.221-224 [Peer Reviewed Journal]

1975 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1975.tb01036.x ;PMID: 1213907

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8
Distribution of break points in reciprocal translocations in children ascertained in population studies
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Article
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Distribution of break points in reciprocal translocations in children ascertained in population studies

Hereditas, 1976-01, Vol.82 (1), p.73-77 [Peer Reviewed Journal]

1976 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1976.tb01541.x ;PMID: 1262241

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9
Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal
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Article
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Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal

Hereditas, 1977-01, Vol.86 (1), p.51-61 [Peer Reviewed Journal]

1977 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1977.tb01212.x ;PMID: 561769

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10
Occupational and environmental risks in and around a smelter in northern Sweden. I. Variations in birth weight
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Occupational and environmental risks in and around a smelter in northern Sweden. I. Variations in birth weight

Hereditas, 1978, Vol.88 (1), p.43-46 [Peer Reviewed Journal]

ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1978.tb01600.x ;PMID: 649423

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11
Occupational and environmental risks in and around a smelter in northern Sweden. VI. Congenital malformations
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Article
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Occupational and environmental risks in and around a smelter in northern Sweden. VI. Congenital malformations

Hereditas, 1979, Vol.90 (2), p.297-302 [Peer Reviewed Journal]

ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1979.tb01317.x ;PMID: 437993

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12
Occupational and environmental risks in and around a smelter in northern Sweden. V. Spontaneous abortion among female employees and decreased birth weight in their offspring
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Article
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Occupational and environmental risks in and around a smelter in northern Sweden. V. Spontaneous abortion among female employees and decreased birth weight in their offspring

Hereditas, 1979, Vol.90 (2), p.291-296 [Peer Reviewed Journal]

ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1979.tb01316.x ;PMID: 437992

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13
A child with partial trisomy 7 and 20 inherited from the mother
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Article
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A child with partial trisomy 7 and 20 inherited from the mother

Hereditas, 1979-01, Vol.91 (1), p.91-95 [Peer Reviewed Journal]

1979 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1979.tb01646.x ;PMID: 500394

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14
Satellite association in human metaphases. A comparative study of normal individuals, patients with Down syndrome and their parents
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Article
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Satellite association in human metaphases. A comparative study of normal individuals, patients with Down syndrome and their parents

Hereditas, 1979-01, Vol.90 (1), p.59-83 [Peer Reviewed Journal]

1979 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1979.tb01294.x ;PMID: 154489

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15
Neonatal X-linked hydrocephalus. Findings in two affected brothers
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Article
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Neonatal X-linked hydrocephalus. Findings in two affected brothers

Hereditas, 1979-09, Vol.91 (1), p.79-82 [Peer Reviewed Journal]

1979 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1979.tb01644.x ;PMID: 500393

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16
Population studies in northern Sweden. IX. Incidence of Down's syndrome by time, region and maternal age
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Article
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Population studies in northern Sweden. IX. Incidence of Down's syndrome by time, region and maternal age

Hereditas, 1979-12, Vol.91 (2), p.257-261 [Peer Reviewed Journal]

1979 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1979.tb01668.x ;PMID: 161302

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17
Transferrin C subtypes in different ethnic groups
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Article
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Transferrin C subtypes in different ethnic groups

Hereditas, 1980-01, Vol.92 (2), p.189-192 [Peer Reviewed Journal]

1980 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1980.tb01694.x ;PMID: 7390866

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18
A fragile secondary constriction on chromosome 2 in five patients with different clinical features
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Article
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A fragile secondary constriction on chromosome 2 in five patients with different clinical features

Hereditas, 1981, Vol.95 (1), p.63-67 [Peer Reviewed Journal]

1981 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1981.tb01329.x ;PMID: 7333874

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19
A child with double trisomy: 48,XYY, + 18
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Article
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A child with double trisomy: 48,XYY, + 18

Hereditas, 1981-01, Vol.95 (1), p.169-171 [Peer Reviewed Journal]

1981 Mendelian Society of Lund ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1981.tb01337.x ;PMID: 7333871

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20
Chromosome abnormalities in newborn children. Aetiological aspects
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Article
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Chromosome abnormalities in newborn children. Aetiological aspects

Hereditas, 1982, Vol.96 (1), p.109-117 [Peer Reviewed Journal]

ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1111/j.1601-5223.1982.tb00042.x ;PMID: 7085336

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