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Items: 18

1.

Craniosynostosis and marfanoid habitus without mental retardation: report of a third case.

Mégarbané A, Hokayem N.

Am J Med Genet. 1998 May 1;77(2):170-1. No abstract available.

PMID:
9605294
2.

Marfanoid features and craniosynostosis: report of one case and review.

Lacombe D, Battin J.

Clin Dysmorphol. 1993 Jul;2(3):220-4. Review.

PMID:
8287183
3.

X-linked mental retardation with marfanoid habitus.

Fryns JP, Buttiens M.

Am J Med Genet. 1987 Oct;28(2):267-74. Review.

PMID:
3322000
4.

Possible third case of Lin-Gettig syndrome.

Hedera P, Innis JW.

Am J Med Genet. 2002 Jul 15;110(4):380-3. Review.

5.

Pseudoaminopterin syndrome.

Verloes A, Bricteux G, Koulischer L.

Am J Med Genet. 1993 Jun 1;46(4):394-7. Review.

PMID:
8357010
6.

Shprintzen-Goldberg syndrome: a clinical analysis.

Greally MT, Carey JC, Milewicz DM, Hudgins L, Goldberg RB, Shprintzen RJ, Cousineau AJ, Smith WL Jr, Judisch GF, Hanson JW.

Am J Med Genet. 1998 Mar 19;76(3):202-12. Review.

PMID:
9508238
7.

[A case of marfanoid body habitus associated with an excessive hyperextensibility of the skin--an unclassified case in inherited connective tissue diseases].

Sakatsume Y, Saito M, Hara Y, Maruno Y, Sato K, Ishii J, Saito N, Hashimoto H, Saito K, Shinkai H.

Nihon Naika Gakkai Zasshi. 1988 Apr;77(4):499-505. Review. Japanese. No abstract available.

PMID:
3042899
8.

[Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].

Liang DS, Wu LQ, Cai F, Xia K, Long ZG, Pan Q, Dai HP, Xia JH.

Yi Chuan Xue Bao. 2005 Feb;32(2):124-9. Review. Chinese.

PMID:
15759858
9.

Shprintzen-Goldberg syndrome: a rare disorder.

Yadav S, Rawal G.

Pan Afr Med J. 2016 Apr 25;23:227. eCollection 2016. Review.

10.

Craniosynostosis syndromes in the genomic era.

Aleck K.

Semin Pediatr Neurol. 2004 Dec;11(4):256-61. Review.

PMID:
15828709
11.

Multiple endocrine neoplasia (MEN)--an overview and case report--patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus.

Fassbender WJ, Krohn-Grimberghe B, Görtz B, Litzlbauer D, Stracke H, Raue F, Kaiser HE.

Anticancer Res. 2000 Nov-Dec;20(6C):4877-87. Review.

PMID:
11205236
12.

Psychopathology in the Lujan-Fryns syndrome: report of two patients and review.

Lerma-Carrillo I, Molina JD, Cuevas-Duran T, Julve-Correcher C, Espejo-Saavedra JM, Andrade-Rosa C, Lopez-Muñoz F.

Am J Med Genet A. 2006 Dec 15;140(24):2807-11. Review.

PMID:
17036352
13.

[Functional retardation in craniosynostosis].

Renier D, Arnaud E, Marchac D.

Neurochirurgie. 2006 Jun;52(2-3 Pt 2):259-63. Review. French. No abstract available.

PMID:
16981658
14.

Michels syndrome, Carnevale syndrome, OSA syndrome, and Malpuech syndrome: variable expression of a single disorder (3MC syndrome)?

Titomanlio L, Bennaceur S, Bremond-Gignac D, Baumann C, Dupuy O, Verloes A.

Am J Med Genet A. 2005 Sep 1;137A(3):332-5. Review.

PMID:
16096999
15.

[Baller-Gerold syndrome].

Satokata I.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):136-7. Review. Japanese. No abstract available.

PMID:
11057169
16.

Clark-Baraitser syndrome: report of a new case and review of the literature.

Mendicino A, Sabbadini G, Pergola MS.

Clin Dysmorphol. 2005 Jul;14(3):133-5. Review.

PMID:
15930902
17.

A new case of Myhre syndrome.

Whiteford ML, Doig WB, Raine PA, Hollman AS, Tolmie JL.

Clin Dysmorphol. 2001 Apr;10(2):135-40. Review.

PMID:
11310994
18.

[Classification of craniosynostosis].

Renier D, Arnaud E, Marchac D.

Neurochirurgie. 2006 Jun;52(2-3 Pt 2):200-27. Review. French. No abstract available.

PMID:
16981654

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