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Items: 1 to 20 of 24

1.

[Familial occurrance of foramina parietalia permagna].

LOTHER K.

Arch Kinderheilkd. 1959;160:156-68. German. No abstract available.

PMID:
14418379
2.

Bone growth in diaphysial aclasis.

SOLOMON L.

J Bone Joint Surg Br. 1961 Nov;43-B:700-16. No abstract available.

3.

Nonfamilial and nonhereditary craniofacial dysostosis: a variant of Crouzon's disease.

DUNN FH.

Am J Roentgenol Radium Ther Nucl Med. 1960 Sep;84:472-8. No abstract available.

PMID:
13818676
4.

WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2).

McGaughran JM, Ward HB, Evans DG.

J Med Genet. 1995 Oct;32(10):823-4. No abstract available.

5.

Genetic heterogeneity in families with hereditary multiple exostoses.

Cook A, Raskind W, Blanton SH, Pauli RM, Gregg RG, Francomano CA, Puffenberger E, Conrad EU, Schmale G, Schellenberg G, et al.

Am J Hum Genet. 1993 Jul;53(1):71-9.

6.

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.

Wu YQ, Heutink P, de Vries BB, Sandkuijl LA, van den Ouweland AM, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJ.

Hum Mol Genet. 1994 Jan;3(1):167-71.

PMID:
8162019
7.

A gene for hereditary multiple exostoses maps to chromosome 19p.

Le Merrer M, Legeai-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P.

Hum Mol Genet. 1994 May;3(5):717-22.

PMID:
8081357
8.

Human haploinsufficiency--one for sorrow, two for joy.

Fisher E, Scambler P.

Nat Genet. 1994 May;7(1):5-7. No abstract available.

PMID:
8075640
9.

A radiation hybrid map of 506 STS markers spanning human chromosome 11.

James MR, Richard CW 3rd, Schott JJ, Yousry C, Clark K, Bell J, Terwilliger JD, Hazan J, Dubay C, Vignal A, et al.

Nat Genet. 1994 Sep;8(1):70-6.

PMID:
7987395
10.
11.
12.

Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.

Lüdecke HJ, Wagner MJ, Nardmann J, La Pillo B, Parrish JE, Willems PJ, Haan EA, Frydman M, Hamers GJ, Wells DE, et al.

Hum Mol Genet. 1995 Jan;4(1):31-6.

PMID:
7711731
13.

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.

Wuyts W, Ramlakhan S, Van Hul W, Hecht JT, van den Ouweland AM, Raskind WH, Hofstede FC, Reyniers E, Wells DE, de Vries B, et al.

Am J Hum Genet. 1995 Aug;57(2):382-7.

14.

Parietal foramina in Saethre-Chotzen syndrome.

Thompson EM, Baraitser M, Hayward RD.

J Med Genet. 1984 Oct;21(5):369-72. No abstract available.

15.

A concordant craniofacial dysostosis with enlarged parietal foramina in twins.

Lehrer HZ, Familant JW.

Radiology. 1969 Jan;92(1):127-9 passim. No abstract available.

PMID:
5762068
16.

Evolution of persistently enlarged parietal foramina.

Murphy J, Gooding CA.

Radiology. 1970 Nov;97(2):391-2. No abstract available.

PMID:
5481147
17.

[Lacunar changes in the parietal bones. Observations on 75 members of a family with an increased occurrece of parietal foramia].

Schmidt-Wittkamp E, Christians H.

Fortschr Geb Rontgenstr Nuklearmed. 1970 Jul;113(1):29-38. German. No abstract available.

PMID:
4994115
18.

Parietal foramina in the Saethre-Chotzen syndrome.

Young ID, Swift PG.

J Med Genet. 1985 Oct;22(5):413-4. No abstract available.

19.

Hereditary enlarged parietal foramina (foramina parietalia permagna). Prenatal diagnosis, evolution and family study.

Rasore-Quartino A, Vignola G, Camera G.

Pathologica. 1985 Jul-Aug;77(1050):449-55. No abstract available.

PMID:
3834376
20.

Familial incidence of foramina parietalia permagna.

Zábek M.

Neurochirurgia (Stuttg). 1987 Jan;30(1):25-7.

PMID:
3561639
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