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2025

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Year Number of Results
1980 1
1987 1
1988 1
1990 2
1996 1
1998 1
2000 4
2001 1
2002 1
2003 1
2008 1
2009 1
2011 1
2018 1
2021 1
2025 0

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18 results

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Page 1
Spontaneous Keloids: A Literature Review.
Jfri A, Alajmi A. Jfri A, et al. Dermatology. 2018;234(3-4):127-130. doi: 10.1159/000491924. Epub 2018 Aug 16. Dermatology. 2018. PMID: 30114700 Review.
RESULTS: Spontaneous keloids have been reported mainly in association with syndromes such as Rubinstein-Taybi syndrome, Dubowitz syndrome, Noonan syndrome, Goeminne syndrome, Bethlem myopathy, conjunctivocorneal dystrophy, X-linked recessive polyfibromatosis and a n …
RESULTS: Spontaneous keloids have been reported mainly in association with syndromes such as Rubinstein-Taybi syndrome, Dubowitz s
[Dubowitz syndrome].
Tsukahara M, Tsujino K. Tsukahara M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(32):295-7. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212722 Review. Japanese. No abstract available.
The Dubowitz syndrome: further observations.
Orrison WW, Schnitzler ER, Chun RW. Orrison WW, et al. Am J Med Genet. 1980;7(2):155-70. doi: 10.1002/ajmg.1320070209. Am J Med Genet. 1980. PMID: 6258433 Review.
An autosomal recessive disorder characterized by intrauterine growth retardation, postnatal retardation, microcephaly, sparse hair, toe syndactyly, and characteristic facial appearance is now recognized as the Dubowitz syndrome. Five addition additional cases of the …
An autosomal recessive disorder characterized by intrauterine growth retardation, postnatal retardation, microcephaly, sparse hair, toe synd …
Congenital atrichia and hypotrichosis.
Bennàssar A, Ferrando J, Grimalt R. Bennàssar A, et al. World J Pediatr. 2011 May;7(2):111-7. doi: 10.1007/s12519-011-0262-z. Epub 2011 May 15. World J Pediatr. 2011. PMID: 21574026 Review.
Fifty years of recognizable patterns of human malformation: Insights and opportunities.
Innes AM, Lynch DC. Innes AM, et al. Am J Med Genet A. 2021 Sep;185(9):2653-2669. doi: 10.1002/ajmg.a.62240. Epub 2021 May 5. Am J Med Genet A. 2021. PMID: 33951288 Review.
Several of the currently "unresolved" syndromes are clinically diverse such as Dubowitz syndrome. Multiple recurrent constellations of embryonic malformations, with VACTERL association as a paradigm, are increasingly likely to have a shared pathogenesis requiring fu …
Several of the currently "unresolved" syndromes are clinically diverse such as Dubowitz syndrome. Multiple recurrent constella …
Microcephaly: general considerations and aids to nosology.
Opitz JM, Holt MC. Opitz JM, et al. J Craniofac Genet Dev Biol. 1990;10(2):175-204. J Craniofac Genet Dev Biol. 1990. PMID: 2211965 Review.
Some cases of syndromal microcephaly may be associated with normal intelligence including some "primordial dwarfs," children with Dubowitz syndrome, FAS, mild SC-Roberts syndrome, and an occasional Brachmann-de Lange individual. ...
Some cases of syndromal microcephaly may be associated with normal intelligence including some "primordial dwarfs," children with Dubowit
The Dubowitz syndrome--one more case.
Chrzanowska KH, Krajewska-Walasek M. Chrzanowska KH, et al. Klin Padiatr. 1987 Sep-Oct;199(5):370-2. doi: 10.1055/s-2008-1026822. Klin Padiatr. 1987. PMID: 3316825 Review.
A boy with the Dubowitz syndrome is presented. This autosomal recessive disorder is characterized by variable degrees of intrauterine and postnatal growth retardation, microcephaly, mild mental retardation, hyperactivity, "eczema", characteristic facial appearance a …
A boy with the Dubowitz syndrome is presented. This autosomal recessive disorder is characterized by variable degrees of intra …
Embryonal rhabdomyosarcoma and chromosomal breakage in a newborn infant with possible Dubowitz syndrome.
Al-Nemri AR, Kilani RA, Salih MA, Al-Ajlan AA. Al-Nemri AR, et al. Am J Med Genet. 2000 May 15;92(2):107-10. doi: 10.1002/(sici)1096-8628(20000515)92:2<107::aid-ajmg5>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10797433 Review.
We report on a newborn girl with Dubowitz syndrome (DS) and embryonal rhabdomyosarcoma (ERMS), with multiple chromosomal breakage (MCB). ...
We report on a newborn girl with Dubowitz syndrome (DS) and embryonal rhabdomyosarcoma (ERMS), with multiple chromosomal break …
[Dubowitz syndrome].
Belohradsky BH, Egger J, Meiswinkel M, Knoop M, Weiss M, Sauer O. Belohradsky BH, et al. Ergeb Inn Med Kinderheilkd. 1988;57:145-84. Ergeb Inn Med Kinderheilkd. 1988. PMID: 3063524 Review. German. No abstract available.
18 results