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Results: 7

Related Articles by Review for PubMed (Select 5807657)

1.

Frontometaphyseal dysplasia. A new syndrome.

Gorlin RJ, Cohen MM Jr.

Am J Dis Child. 1969 Sep;118(3):487-94. No abstract available.

PMID:
5807657
2.

Central nervous system malformations, dense bones and facial dysmorphism: a new autosomal recessive syndrome.

al-Gazali LI, Bakalinova D, Bakir M.

Clin Dysmorphol. 1998 Apr;7(2):123-6. Review.

PMID:
9571283
3.

Characteristic facial dysmorphism, arachnodactyly and mental retardation: another case.

Van Buggenhout GJ, Akkermans-Scholten AC, Hamel BC.

Genet Couns. 1995;6(1):61-3. Review. No abstract available.

PMID:
7794564
4.

Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.

Kulharya AS, Maberry M, Kukolich MK, Day DW, Schneider NR, Wilson GN, Tonk V.

Am J Med Genet. 1995 Jan 16;55(2):165-70. Review.

PMID:
7717415
5.

Rieger's syndrome: a case report.

Prabhu NT, John R, Munshi AK.

Quintessence Int. 1997 Nov;28(11):749-52. Review.

PMID:
9573866
6.

Ectodermal abnormalities in Kabuki syndrome.

Lerone M, Priolo M, Naselli A, Vignolo M, Romeo G, Silengo MC.

Am J Med Genet. 1997 Dec 19;73(3):263-6. Review.

PMID:
9415681
7.

[Oculo-osteo-cutaneous syndrome, Toumaala-Haapanen type].

Numabe H.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):354-5. Review. Japanese. No abstract available.

PMID:
11528780
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