Literature DB >> 13030518

A clinical and genetical study of microcephaly.

J A BOOK, J W SCHUT, S C REED.   

Abstract

Keywords:  MICROCEPHALY

Mesh:

Year:  1953        PMID: 13030518

Source DB:  PubMed          Journal:  Am J Ment Defic        ISSN: 0002-9351


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  12 in total

1.  [Chromosomal instability in homo- and heterocygocity for microcephalia vera )author's transl)].

Authors:  W Vormittag; E Kunze-Mühl; M Weninger
Journal:  Humangenetik       Date:  1975

2.  DISCORDANCE IN MONOZYGOTIC TWINS: ONE DIABETIC, THE OTHER AN IDIOT WITH NEUROLOGICAL ABNORMALITIES.

Authors:  N PARKER
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

3.  Genetic study of microcephaly based on Japanese material.

Authors:  T KOMAI; K KISHIMOTO; Y OZAKI
Journal:  Am J Hum Genet       Date:  1955-03       Impact factor: 11.025

4.  Microcephaly in one of monozygous twins.

Authors:  M G BRANDON; B H KIRMAN; C E WILLIAMS
Journal:  Arch Dis Child       Date:  1959-02       Impact factor: 3.791

5.  [Familial microcephalies due to cerebral malformation. Anatomical and clinical study].

Authors:  O Robain; G Lyon
Journal:  Acta Neuropathol       Date:  1972       Impact factor: 17.088

6.  Apparent microcephaly caused by a bicornuate uterus.

Authors:  R M Winter; J Dearlove; H Jolly; M Pawson; R G Wilson
Journal:  Br Med J (Clin Res Ed)       Date:  1983-05-21

Review 7.  Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

Authors:  C Geoffrey Woods; Jacquelyn Bond; Wolfgang Enard
Journal:  Am J Hum Genet       Date:  2005-03-31       Impact factor: 11.025

8.  A biometric analysis of brain size in micrencephalics.

Authors:  M A Hofman
Journal:  J Neurol       Date:  1984       Impact factor: 4.849

9.  Autosomal dominant isolated ('uncomplicated') microcephaly.

Authors:  P Merlob; D Steier; S H Reisner
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

10.  Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anemia, and xeroderma pigmentosum families.

Authors:  K Welshimer; M Swift
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

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