Literature DB >> 4365204

Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.

J M Opitz, E G Kaveggia.   

Abstract

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Year:  1974        PMID: 4365204     DOI: 10.1007/bf00439020

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN: 0044-2917


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  12 in total

1.  SEX-LINKED IMPERFORATE ANUS.

Authors:  E D WEINSTEIN
Journal:  Pediatrics       Date:  1965-04       Impact factor: 7.124

2.  Agenesis of the corpus callosum; a report of two cases in siblings.

Authors:  J NAIMAN; F C FRASER
Journal:  AMA Arch Neurol Psychiatry       Date:  1955-08

3.  Congenital absence of the corpus callosum; report of a case and review of the literature.

Authors:  U T SLAGER; A B KELLY; J A WAGNER
Journal:  N Engl J Med       Date:  1957-06-20       Impact factor: 91.245

4.  [Malignant familial early infantile convulsive disoders, partial relation with aplasia of corpus callosum].

Authors:  E ZIEGLER
Journal:  Helv Paediatr Acta       Date:  1958-04

5.  Agenesis of the corpus callosum; a study of 18 cases diagnosed during life.

Authors:  M B CARPENTER
Journal:  Neurology       Date:  1954-03       Impact factor: 9.910

6.  Agenesis of the corpus callosum with concomitant malformations, including atresia of the foramens of Luschka and Magendie.

Authors:  E F VAN EPPS
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1953-07

7.  Agenesis of the corpus callosum diagnosed during life; review of the literature and presentation of two cases.

Authors:  M B CARPENTER; W H DRUCKEMILLER
Journal:  AMA Arch Neurol Psychiatry       Date:  1953-03

8.  Mid-line anomalies of the brain; their diagnosis by pneumoencephalography.

Authors:  A P ECHTERNACHT; J A CAMPBELL
Journal:  Radiology       Date:  1946-02       Impact factor: 11.105

9.  [Agenesis of the corpus callosum].

Authors:  H ZELLWEGER
Journal:  Helv Paediatr Acta       Date:  1952-04

10.  Agenesis of the corpus callosum in two sisters.

Authors:  Y Shapira; T Cohen
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

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  27 in total

1.  2011 William Allan Award introduction: John M. Opitz.

Authors:  Maximilian Muenke
Journal:  Am J Hum Genet       Date:  2012-03-09       Impact factor: 11.025

Review 2.  MED12 mutations in human diseases.

Authors:  Hua Wang; Qin Shen; Li-Hua Ye; Jun Ye
Journal:  Protein Cell       Date:  2013-09       Impact factor: 14.870

Review 3.  MED12 related disorders.

Authors:  John M Graham; Charles E Schwartz
Journal:  Am J Med Genet A       Date:  2013-10-10       Impact factor: 2.802

4.  Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

Authors:  S R Dlouhy; J C Christian; J L Haines; P M Conneally; M E Hodes
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

5.  Necropsy findings in a child with FG syndrome.

Authors:  E M Thompson; B N Harding; B D Lake; S C Smith
Journal:  J Med Genet       Date:  1986-08       Impact factor: 6.318

6.  FG syndrome.

Authors:  E Thompson; M Baraitser
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

7.  Two retarded male cousins with odd facies, hypotonia, and severe constipation: possible examples of the X linked FG syndrome.

Authors:  J Burn; N Martin
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

8.  X linked recessive inheritance of agenesis of the corpus callosum.

Authors:  P Kaplan
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

Review 9.  Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome).

Authors:  John M Graham; Robin D Clark; John B Moeschler; R Curtis Rogers
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-11-15       Impact factor: 3.908

10.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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