Literature DB >> 5480960

Absent IgA and deletions of chromosome 18.

J M Stewart, S Go, E Ellis, A Robinson.   

Abstract

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Year:  1970        PMID： 5480960      PMCID： PMC1468899          DOI： 10.1136/jmg.7.1.11

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  55 in total

1.  Lack of gamma A-immunoglobulin in serum of patients with steatorrhoea.

Authors:  P A Crabbé; J F Heremans
Journal:  Gut       Date:  1966-04       Impact factor: 23.059

2.  Electroimmunodiffusion (EID): a simple, rapid method for quantitation of immunoglobulins in dilute biological fluids.

Authors:  D Merrill; T F Hartley; H N Claman
Journal:  J Lab Clin Med       Date:  1967-01

3.  Syndrome associated with a deficiency of part of the long arm of chromosome no. 18.

Authors:  J Insley
Journal:  Arch Dis Child       Date:  1967-04       Impact factor: 3.791

4.  Protective effect of antibody to parainfluenza type 1 virus.

Authors:  C B Smith; R H Purcell; J A Bellanti; R M Chanock
Journal:  N Engl J Med       Date:  1966-11-24       Impact factor: 91.245

5.  Immunochemical quantitation of antigens by single radial immunodiffusion.

Authors:  G Mancini; A O Carbonara; J F Heremans
Journal:  Immunochemistry       Date:  1965-09

6.  Studies on the serum gamma-A-globulin level. 3. The frequency of A-gamma-A-globulinemia.

Authors:  R Bachmann
Journal:  Scand J Clin Lab Invest       Date:  1965       Impact factor: 1.713

7.  Short arm deletions in group E and chromosomal "deletion" syndromes.

Authors:  B R Migeon
Journal:  J Pediatr       Date:  1966-09       Impact factor: 4.406

8.  Serum immunoglobulin measurement during the first year of life and in immunoglobulin-deficiency states.

Authors:  V A Fulginiti; O F Sieber; H N Claman; D Merrill
Journal:  J Pediatr       Date:  1966-05       Impact factor: 4.406

9.  Partial 18 monosomy in the cyclops malformation.

Authors:  H M Nitowsky; N Sindhvananda; U R Konigsberg; T Weinberg
Journal:  Pediatrics       Date:  1966-02       Impact factor: 7.124

10.  A ring D chromosome and anomalous inheritance of haptoglobin type.

Authors:  P S Gerald; S Warner; J D Singer; P A Corcoran; I Umansky
Journal:  J Pediatr       Date:  1967-02       Impact factor: 4.406
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  12 in total

1.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  Immunoglobulin abnormality in a girl with a large chromosome 18.

Authors:  S Yanagisawa
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

6.  Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18.

Authors:  J Leisti; S Leisti; J Perheentupa; E Savilahti; P Aula
Journal:  Arch Dis Child       Date:  1973-04       Impact factor: 3.791

7.  IgA deficiency in children. A clinical study with special reference to intestinal findings.

Authors:  E Savilahti; P Pelkonen; J K Visakorpi
Journal:  Arch Dis Child       Date:  1971-10       Impact factor: 3.791

8.  Familial mental retardation in a family with an inherited chromosome rearrangement.

Authors:  A E Chudley; F Bauder; M Ray; P J McAlpine; S D Pena; J L Hamerton
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

9.  Genetic aspects of selective immunoglobulin A deficiency.

Authors:  F J Grundbacher
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

10.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975
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