Literature DB >> 13444248

The laboratory detection of heterozygotes.

D Y HSIA.   

Abstract

Keywords:  GENETICS

Mesh:

Year:  1957        PMID: 13444248      PMCID: PMC1931845     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  74 in total

1.  Hereditary spherocytosis.

Authors:  L E YOUNG
Journal:  Am J Med       Date:  1955-03       Impact factor: 4.965

2.  Genetic, clinical, biochemical, and pathological features of hypophosphatasia; based on the study of a family.

Authors:  A M BARRETT; D V FAIRWEATHER; R A MCCANCE; A B MORRISON
Journal:  Q J Med       Date:  1956-10

3.  A laboratory study of the carrier state in classic hemophilia.

Authors:  A MARGOLIUS; O D RATNOFF
Journal:  J Clin Invest       Date:  1956-11       Impact factor: 14.808

4.  The carrier state in nephrogenic diabetes insipidus.

Authors:  C CARTER; M SIMPKISS
Journal:  Lancet       Date:  1956-11-24       Impact factor: 79.321

5.  Glycogen-storage disease of liver.

Authors:  C C KAPILA; S KAUL; B C CHATTERJEE
Journal:  Br Med J       Date:  1956-04-21

6.  Studies on agammaglobulinemia. II. Failure of plasma cell formation in the bone marrow and lymph nodes of patients with agammaglobulinemia.

Authors:  R A GOOD
Journal:  J Lab Clin Med       Date:  1955-08

7.  Studies on the metabolism of adrenal steroids in the adrenogenital syndrome.

Authors:  A M BONGIOVANNI; W R EBERLEIN; J CARA
Journal:  J Clin Endocrinol Metab       Date:  1954-04       Impact factor: 5.958

8.  Congenital familial nonhemolytic jaundice with kernicterus.

Authors:  J F CRIGLER; V A NAJJAR
Journal:  Pediatrics       Date:  1952-08       Impact factor: 7.124

9.  Hypercholesteremia with predisposition to atherosclerosis, an inborn error of lipid metabolism.

Authors:  D ADLERSBERG
Journal:  Am J Med       Date:  1951-11       Impact factor: 4.965

10.  Parahemophilia in three siblings (Owren's disease).

Authors:  B ALEXANDER; R GOLDSTEIN
Journal:  Am J Med       Date:  1952-09       Impact factor: 4.965

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  5 in total

1.  Idiopathic hyperlipemia. A case report in a nine-year-old Negro girl with an associated deficiency in labile factor and prothrombin.

Authors:  S HARA; G E ACKAOUY; E P CRUMP
Journal:  J Natl Med Assoc       Date:  1962-09       Impact factor: 1.798

2.  Hypocatalasemia: a new genetic carrier state.

Authors:  S TAKAHARA; H B HAMILTON; J V NEEL; T Y KOBARA; Y OGURA; E T NISHIMURA
Journal:  J Clin Invest       Date:  1960-04       Impact factor: 14.808

3.  Mendelian Terms in Modern Genetics-An Anachronism?

Authors:  G Allen
Journal:  Am J Hum Genet       Date:  1958-09       Impact factor: 11.025

4.  Cystic fibrosis: A community challenge.

Authors:  L L Kulczucki; K I E Macleod
Journal:  Public Health Rep       Date:  1961-01       Impact factor: 2.792

5.  Heterozygous carriers of Nijmegen Breakage Syndrome have a distinct gene expression phenotype.

Authors:  Vivian G Cheung; Warren J Ewens
Journal:  Genome Res       Date:  2006-06-29       Impact factor: 9.043

  5 in total

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