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Items: 1 to 20 of 202

1.

Mesomelic dwarfism as the homozygous expression of dyschondrosteosis.

Espiritu C, Chen H, Woolley PV Jr.

Am J Dis Child. 1975 Mar;129(3):375-7. No abstract available.

PMID:
1121969
2.

[Mesomelic dwarfism of the Langer type as a homozygous form of dyschondrosteosis (author's transl)].

Kemperdick H, Majewski F.

Rofo. 1982 May;136(5):583-7. German. No abstract available.

PMID:
6212507
3.

Dyschondrosteosis (mesomelic dwarfism)--a family study.

Carter AR, Currey HL.

Br J Radiol. 1974 Oct;47(562):634-40. No abstract available.

PMID:
4433973
4.

Mesomelic dwarfism of the hypoplastic ulna, fibula, mandible type.

Langer LO Jr.

Radiology. 1967 Oct;89(4):654-60. No abstract available.

PMID:
6059604
5.

Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis.

Fryns JP, Van Den Berghe H.

Hum Genet. 1979 Jan 19;46(1):21-7.

PMID:
429003
6.

[Leri-Weill's dyschondrosteosis].

Muzzo S, Castillo C, Burrows R.

Rev Chil Pediatr. 1985 May-Jun;56(3):184-7. Spanish. No abstract available.

PMID:
4095311
7.

Mesomelic dysplasia: Langer type.

Baxova A, Kozlowski K, Netriova I, Sillence D.

Australas Radiol. 1994 Feb;38(1):58-60.

PMID:
8147804
8.

Dyschondrosteosis. A Mexican family with two affected males.

Lisker R, Gamboa I, Hernández J.

Clin Genet. 1972;3(3):154-7. No abstract available.

PMID:
5054807
9.

A family with concurrent mesomelic shortening and hereditary nephritis.

Funderburk SJ, Smith L, Falk RE, Bergstein JM, Winter H.

Birth Defects Orig Artic Ser. 1976;12(6):47-61. Review. No abstract available.

PMID:
788812
10.

Mesomelic dysplasia, type Langer--a homozygous state for dyschondrosteosis.

Kunze J, Klemm T.

Eur J Pediatr. 1980 Sep;134(3):269-72.

PMID:
7428776
11.

Congenital conductive hearing loss in dyschondrosteosis.

De Leenheer EM, Oudesluijs GG, Kuijpers-Jagtman AM, Rappold GA, Sengers RC, Cremers CW.

Ann Otol Rhinol Laryngol. 2003 Feb;112(2):153-8.

PMID:
12597288
12.

[Study of the classification of chondrodysplasias with mesomelic predominance].

Maroteaux P, Spranger J.

Arch Fr Pediatr. 1977 Dec;34(10):945-58. French.

PMID:
610660
13.

Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature.

Beals RK, Lovrien EW.

Clin Orthop Relat Res. 1976 May;(116):24-8.

PMID:
1277646
14.

[Ulno-fibular dysplasia. An autosome-dominant hereditary micromesomelia resembling the Nievergelt syndrome].

Reinhardt K, Pfeiffer RA.

Fortschr Geb Rontgenstr Nuklearmed. 1967 Sep;107(3):379-91. German. No abstract available.

PMID:
5626375
15.

Father to son transmission in metaphyseal chondrodysplasia mimicking vitamin D resistant rickets.

Held KR, Riebel T, Schaefer E.

Prog Clin Biol Res. 1982;104:143-8. No abstract available.

PMID:
6298812
16.

[Mesomelic dwarfism (author's transl)].

Kemperdick H, Janssen F, Lenz W.

Rofo. 1975 Nov;123(5):450-4. German.

PMID:
128504
17.

Madelung's disease of the wrist and dyschondrosteosis.

Golding JS, Blackburne JS.

J Bone Joint Surg Br. 1976 Aug;58(3):350-2.

18.

Probable homozygosity for the dyschondrosteosis genes.

Espiritu CE, Chen H, Woolley PV Jr.

Birth Defects Orig Artic Ser. 1975;11(6):127-32. No abstract available.

PMID:
1201337
19.

[Observation of twins in familial dyschondrosteosis (a contribution on the knowledge of Léri-Weill disease)].

Thiel HV, Berquet KH.

Arch Orthop Unfallchir. 1969;65(2):182-8. German. No abstract available.

PMID:
5778521
20.

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