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Items: 5

1.

Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.

Zweier C, Rittinger O, Bader I, Berland S, Cole T, Degenhardt F, Di Donato N, Graul-Neumann L, Hoyer J, Lynch SA, Vlasak I, Wieczorek D.

Am J Med Genet C Semin Med Genet. 2014 Sep;166C(3):290-301. doi: 10.1002/ajmg.c.31408. Epub 2014 Aug 5. Review.

PMID:
25099957
2.

[Börjeson-Forssman-Lehmann syndrome].

Kubota T.

Nihon Rinsho. 2006 Sep 28;Suppl 3:410-2. Review. Japanese. No abstract available.

PMID:
17022575
3.

[Börjeson-Forssman-Lehmann syndrome].

Kubota T.

Ryoikibetsu Shokogun Shirizu. 2001;(33):284-5. Review. Japanese. No abstract available.

PMID:
11462441
4.

[Börjeson-Forssman-Lehmann syndrome].

Fujieda K.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):147-9. Review. Japanese. No abstract available.

PMID:
11057174
5.

Prader-Willi and other syndromes associated with obesity and mental retardation.

Gunay-Aygun M, Cassidy SB, Nicholls RD.

Behav Genet. 1997 Jul;27(4):307-24. Review.

PMID:
9519559

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