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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1977 | 1 |
1984 | 1 |
1994 | 2 |
2000 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 66317
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The KBG syndrome.
Clin Dysmorphol. 2000 Apr;9(2):87-91. doi: 10.1097/00019605-200009020-00002.
Clin Dysmorphol. 2000.
PMID: 10826617
Review.
The KBG syndrome: follow-up data on three affected brothers.
Soekarman D, Volcke P, Fryns JP.
Soekarman D, et al.
Clin Genet. 1994 Oct;46(4):283-6. doi: 10.1111/j.1399-0004.1994.tb04160.x.
Clin Genet. 1994.
PMID: 7834892
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Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.
Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G.
Zollino M, et al.
Am J Med Genet. 1994 Sep 1;52(3):302-7. doi: 10.1002/ajmg.1320520310.
Am J Med Genet. 1994.
PMID: 7810561
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Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome?
Fryns JP, Haspeslagh M.
Fryns JP, et al.
Clin Genet. 1984 Jul;26(1):69-72. doi: 10.1111/j.1399-0004.1984.tb00792.x.
Clin Genet. 1984.
PMID: 6467660
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Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred. A variant of K.B.G. syndrome or a new mental retardation syndrome.
Parloir C, Fryns JP, Deroover J, Lebas E, Goffaux P, van den Berghe H.
Parloir C, et al.
Clin Genet. 1977 Nov;12(5):263-6. doi: 10.1111/j.1399-0004.1977.tb00939.x.
Clin Genet. 1977.
PMID: 589847
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