Literature DB >> 3572995

FG syndrome.

E Thompson, M Baraitser.   

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Year:  1987        PMID： 3572995      PMCID： PMC1049945          DOI： 10.1136/jmg.24.3.139

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


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  9 in total

1.  A new syndrome of mental deficiency with craniofacial, limb, and anal abnormalities.

Authors:  M A Keller; K L Jones; W L Nyhan; U Francke; B Dixson
Journal:  J Pediatr       Date:  1976-04       Impact factor: 4.406

2.  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

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

Authors:  J M Opitz; E G Kaveggia
Journal:  Z Kinderheilkd       Date:  1974-04-08

4.  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

5.  Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG family.

Authors:  J M Opitz; E G Kaveggia; W N Adkins; E F Gilbert; C Viseskul; J C Pettersen; B Blumberg
Journal:  Am J Med Genet       Date:  1982-06

6.  The FG syndrome: 7 new cases.

Authors:  E M Thompson; M Baraitser; R H Lindenbaum; Z H Zaidi; J S Kroll
Journal:  Clin Genet       Date:  1985-06       Impact factor: 4.438

7.  Sensorineural deafness in the FG syndrome: report on four new cases.

Authors:  G Neri; B Blumberg; P V Miles; J M Opitz
Journal:  Am J Med Genet       Date:  1984-10

8.  FG syndrome in a premature male.

Authors:  D W Bianchi
Journal:  Am J Med Genet       Date:  1984-10

9.  The FG syndrome: further characterization, report of a third family, and of a sporadic case.

Authors:  V M Riccardi; E Hässler; M S Lubinsky
Journal:  Am J Med Genet       Date:  1977
  9 in total
  5 in total

Review 1.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

2.  The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

Authors:  P Saugier-Veber; V Abadie; A Moncla; M Mathieu; C Piussan; C Turleau; J F Mattei; A Munnich; S Lyonnet
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

3.  X linked mental retardation: a family with a separate syndrome?

Authors:  E M Thompson; A Gordon; M Baraitser
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

Review 4.  Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise.

Authors:  A H Lipson; D Yuille; M Angel; P G Thompson; J G Vandervoord; E J Beckenham
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318

5.  Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?

Authors:  J J Jonsson; A Renieri; P G Gallagher; C E Kashtan; E M Cherniske; M Bruttini; M Piccini; F Vitelli; A Ballabio; B R Pober
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318
  5 in total

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