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Items: 16

1.

Cranio-carpo-tarsal dysplasia or the whistling face syndrome. II. Oral intercommissural distance in children.

Cervenka J, Figalová P, Gorlin RJ.

Am J Dis Child. 1969 Apr;117(4):434-5. No abstract available.

PMID:
5773411
2.

9q34.3 deletion syndrome in three unrelated children.

Iwakoshi M, Okamoto N, Harada N, Nakamura T, Yamamori S, Fujita H, Niikawa N, Matsumoto N.

Am J Med Genet A. 2004 Apr 30;126A(3):278-83. Review.

PMID:
15054842
3.

Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study.

Fleck BJ, Pandya A, Vanner L, Kerkering K, Bodurtha J.

Am J Med Genet. 2001 Feb 15;99(1):1-7. Review.

PMID:
11170086
4.

X-chromosome polysomy in the female: personal experience and review of the literature.

Fryns JP, Kleczkowska A, Petit P, van den Berghe H.

Clin Genet. 1983 May;23(5):341-9. Review. No abstract available.

PMID:
6342877
5.

[Molecular diagnosis of CHARGE syndrom].

Pedersen AM, Skovby F.

Ugeskr Laeger. 2007 Jan 29;169(5):402-6. Review. Danish.

PMID:
17280632
6.

Filippi syndrome: report of three additional cases.

Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.

Am J Med Genet. 1999 Nov 19;87(2):128-33. Review.

PMID:
10533026
7.

Whistling face syndrome. A case report and literature review.

Millner MM, Mutz ID, Rosenkranz W.

Acta Paediatr Hung. 1991;31(3):279-89. Review.

PMID:
1742043
8.

[Considerations on lipomatosis of the tongue in the framework of orofaciodigital syndrome].

Berger PE, Dambrain R, Peiffer R.

Acta Stomatol Belg. 1967;64(2):207-31. Review. French. No abstract available.

PMID:
4861315
9.

[Cranio-carpo-tarsal dysplasia, whistling face type].

Kawame H.

Ryoikibetsu Shokogun Shirizu. 2001;(33):501-2. Review. Japanese. No abstract available.

PMID:
11462538
10.

W syndrome: report of three cases and review.

Goizet C, Bonneau D, Lacombe D.

Am J Med Genet. 1999 Dec 22;87(5):446-9. Review.

PMID:
10594887
11.

Terminal deletion of the long arm of chromosome 4 in a mother and two sons.

Descartes M, Keppler-Noreuil K, Knops J, Longshore JW, Finley WH, Carroll AJ.

Clin Genet. 1996 Dec;50(6):538-40. Review.

PMID:
9147894
12.

Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.

Ramer JC, Lin AE, Dobyns WB, Winter R, Aymé S, Pallotta R, Ladda RL.

Am J Med Genet. 1995 Jul 3;57(3):403-9. Review.

PMID:
7545868
13.

Interstitial deletion (6)q13q15.

Gershoni-Baruch R, Mandel H, Bar El H, Bar-Nizan N, Borochowitz Z, Dar H.

Am J Med Genet. 1996 Apr 24;62(4):345-7. Review.

PMID:
8723062
14.

Pitt-Rogers-Danks syndrome: further delineation.

Lizcano-Gil LA, García-Cruz D, García-Cruz O, Sánchez-Corona J.

Am J Med Genet. 1995 Feb 13;55(4):420-2. Review.

PMID:
7762580
15.

[Orofaciodigital syndrome].

Gombos F, Serpico R, Zambrano S.

Arch Stomatol (Napoli). 1988 Dec;29(6):1217-27. Review. Italian.

PMID:
3079106
16.

Intellectual development and the OFD syndrome: a review.

Ruess AL, Pruzansky S, Lis EF.

Cleft Palate J. 1965 Oct;2:350-6. Review. No abstract available.

PMID:
5318798

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