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Results: 1 to 20 of 37

Related Articles by Review for PubMed (Select 16293761)

1.

GTF2IRD1 in craniofacial development of humans and mice.

Tassabehji M, Hammond P, Karmiloff-Smith A, Thompson P, Thorgeirsson SS, Durkin ME, Popescu NC, Hutton T, Metcalfe K, Rucka A, Stewart H, Read AP, Maconochie M, Donnai D.

Science. 2005 Nov 18;310(5751):1184-7. Epub 2005 Nov 3.

2.

The genetic basis of normal and abnormal craniofacial development.

Thesleff I.

Acta Odontol Scand. 1998 Dec;56(6):321-5. Review.

PMID:
10066109
3.

Neurodevelopmental and behavioral issues in Williams syndrome.

Paterson SJ, Schultz RT.

Curr Psychiatry Rep. 2007 Apr;9(2):165-71. Review.

PMID:
17389129
4.

Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.

Tassabehji M.

Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R229-37. Epub 2003 Sep 2. Review.

5.

Familial Williams-Beuren syndrome showing varying clinical expression.

Pankau R, Siebert R, Kautza M, Schneppenheim R, Gosch A, Wessel A, Partsch CJ.

Am J Med Genet. 2001 Feb 1;98(4):324-9. Review.

PMID:
11170076
6.

Williams-Beuren syndrome: an update and review for the primary physician.

Lashkari A, Smith AK, Graham JM Jr.

Clin Pediatr (Phila). 1999 Apr;38(4):189-208. Review.

PMID:
10326175
7.

[Williams-Beuren syndrome].

Gilbert-Dussardier B.

Rev Prat. 2006 Dec 15;56(19):2102-6. Review. French.

PMID:
17416045
8.

Molecular biology experimental strategies for craniofacial-oral-dental dysmorphology.

Slavkin HC.

Connect Tissue Res. 1995;32(1-4):233-9. Review.

PMID:
7554921
9.

[Williams-Beuren syndrome: a multidisciplinary approach].

Lacroix A, Pezet M, Capel A, Bonnet D, Hennequin M, Jacob MP, Bricca G, Couet D, Faury G, Bernicot J, Gilbert-Dussardier B.

Arch Pediatr. 2009 Mar;16(3):273-82. doi: 10.1016/j.arcped.2008.11.011. Epub 2008 Dec 18. Review. French.

PMID:
19097873
10.

SAMS, a syndrome of short stature, auditory-canal atresia, mandibular hypoplasia, and skeletal abnormalities is a unique neurocristopathy caused by mutations in Goosecoid.

Parry DA, Logan CV, Stegmann AP, Abdelhamed ZA, Calder A, Khan S, Bonthron DT, Clowes V, Sheridan E, Ghali N, Chudley AE, Dobbie A, Stumpel CT, Johnson CA.

Am J Hum Genet. 2013 Dec 5;93(6):1135-42. doi: 10.1016/j.ajhg.2013.10.027. Epub 2013 Nov 27. Review.

11.

The genomic basis of the Williams-Beuren syndrome.

Schubert C.

Cell Mol Life Sci. 2009 Apr;66(7):1178-97. doi: 10.1007/s00018-008-8401-y. Review.

PMID:
19039520
12.

Genetics of craniofacial development and malformation.

Wilkie AO, Morriss-Kay GM.

Nat Rev Genet. 2001 Jun;2(6):458-68. Review.

PMID:
11389462
13.

Recent advances in craniofacial morphogenesis.

Chai Y, Maxson RE Jr.

Dev Dyn. 2006 Sep;235(9):2353-75. Review.

14.

Delineation of the proximal 3q microdeletion syndrome.

Simovich MJ, Bland SD, Peiffer DA, Gunderson KL, Cheung SW, Yatsenko SA, Shinawi M.

Am J Med Genet A. 2008 Jul 1;146A(13):1729-35. doi: 10.1002/ajmg.a.32292. Review.

PMID:
18536049
15.

[Genetics and language in Williams-Beuren Syndrome: a distinct neurobehavioral disorder].

Rossi NF, Moretti-Ferreira D, Giacheti CM.

Pro Fono. 2006 Sep-Dec;18(3):331-8. Review. Portuguese.

PMID:
17180802
16.

Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.

Stalmans I.

Verh K Acad Geneeskd Belg. 2005;67(4):229-76. Review.

PMID:
16334858
17.

Diagnosis and management of medical problems in adults with Williams-Beuren syndrome.

Pober BR, Morris CA.

Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):280-90. Review.

PMID:
17639596
18.

[Genetics of craniofacial development].

van Adrichem LN, Hoogeboom AJ, Wolvius EB.

Ned Tijdschr Tandheelkd. 2008 Feb;115(2):61-8. Review. Dutch.

PMID:
18326400
19.

Form and function in craniofacial deformities.

Beals SP, Joganic EF.

Semin Pediatr Neurol. 2004 Dec;11(4):238-42. Review.

PMID:
15828706
20.

Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder.

Kaplan P, Wang PP, Francke U.

J Child Neurol. 2001 Mar;16(3):177-90. Review. No abstract available.

PMID:
11305686
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