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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
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The detection of the genetic carriers of hereditary diseaseAmerican journal of human genetics, 1949-09, Vol.1 (1), p.19-36 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948380Full text available |
| 2 |
Material Type: Article
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Hereditary congenital macular degenerationAmerican journal of human genetics, 1949-09, Vol.1 (1), p.96-104 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948388Full text available |
| 3 |
Material Type: Article
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Hereditary nerve deafnessAmerican journal of human genetics, 1949-09, Vol.1 (1), p.37-51 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948381Full text available |
| 4 |
Material Type: Article
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Chromatid bridges and fragments in human spermatocytesAmerican journal of human genetics, 1949-09, Vol.1 (1), p.79-82 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948385Full text available |
| 5 |
Material Type: Article
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Progress and prospects in human geneticsAmerican journal of human genetics, 1949-09, Vol.1 (1), p.1-18 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948379Full text available |
| 6 |
Material Type: Article
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Paget's disease (Osteitis deformans) and heredityAmerican journal of human genetics, 1949-09, Vol.1 (1), p.94-95 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948387Full text available |
| 7 |
Material Type: Article
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Rh-incompatibility and mental deficiencyAmerican journal of human genetics, 1949-09, Vol.1 (1), p.66-78 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948384Full text available |
| 8 |
Material Type: Article
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Sex-linked nystagmus associated with red-green color-blindnessAmerican journal of human genetics, 1949-09, Vol.1 (1), p.52-54 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948382Full text available |
| 9 |
Material Type: Article
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The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutationsAmerican journal of human genetics, 1949-12, Vol.1 (2), p.156-178 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948392Full text available |
| 10 |
Material Type: Article
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Suicide in twins and only childrenAmerican journal of human genetics, 1949-12, Vol.1 (2), p.113-126 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948389Full text available |
| 11 |
Material Type: Article
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Note on the genetics of acrokeratosis verruciformis (Hopf)American journal of human genetics, 1949-12, Vol.1 (2), p.214-215 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948395Full text available |
| 12 |
Material Type: Article
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Rh nomenclatureAmerican journal of human genetics, 1949-12, Vol.1 (2), p.215-218 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948396Full text available |
| 13 |
Material Type: Article
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Turner's syndrome and status bonnevie-ullrich; A synthesis of animal phenogenetics and clinical observations on a typical complex of developmental anomaliesAmerican journal of human genetics, 1949-12, Vol.1 (2), p.179-202 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948393Full text available |
| 14 |
Material Type: Article
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Unilateral developmental anomalies in sistersAmerican journal of human genetics, 1949-12, Vol.1 (2), p.203-213 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 17948394Full text available |
| 15 |
Material Type: Article
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Breast cancer in one family groupAmerican journal of human genetics, 1950-03, Vol.2 (1), p.30-40 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 15425503Full text available |
| 16 |
Material Type: Article
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Cancer of the lower digestive tract in one family groupAmerican journal of human genetics, 1950-03, Vol.2 (1), p.41-48 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 15425504Full text available |
| 17 |
Material Type: Article
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Gaucher's disease: cases in 5 related Negro sibshipsAmerican journal of human genetics, 1950-03, Vol.2 (1), p.49-60 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 15425505Full text available |
| 18 |
Material Type: Article
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A clinical and genetical study of anencephalyAmerican journal of human genetics, 1950-03, Vol.2 (1), p.61 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 15425506Full text available |
| 19 |
Material Type: Article
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Late cortical cerebellar atrophy, a form of hereditary cerebellar ataxiaAmerican journal of human genetics, 1950-03, Vol.2 (1), p.1-29 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 15425502Full text available |
| 20 |
Material Type: Article
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Our load of mutationsAmerican journal of human genetics, 1950-06, Vol.2 (2), p.111-176 [Peer Reviewed Journal]ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 14771033Full text available |
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