274 related articles for article (PubMed ID: 128504)
1. [Mesomelic dwarfism (author's transl)].
Kemperdick H; Janssen F; Lenz W
Rofo; 1975 Nov; 123(5):450-4. PubMed ID: 128504
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 6212507
[No Abstract] [Full Text] [Related]
3. [Familial mesomelial dwarfism (Nievergelt syndrome)].
Hess OM; Goebel NH; Streuli R
Schweiz Med Wochenschr; 1978 Aug; 108(31):1202-6. PubMed ID: 675214
[TBL] [Abstract][Full Text] [Related]
4. [Mesomelic dwarfism Langer type associated to mixed gonadal dysgenesis, whit cariotipe 46,XY/45 X (author's transl)].
Ruíz Gómez MJ; Martínez González M; Machín Jiménez AR; Fernández Villahoz AL
An Esp Pediatr; 1979 Dec; 12(12):897-904. PubMed ID: 533057
[TBL] [Abstract][Full Text] [Related]
5. Nievergelt syndrome (mesomelic dwarfism-type Nievergelt).
Young LW; Wood BP
Birth Defects Orig Artic Ser; 1974; 10(5):81-6. PubMed ID: 4469999
[No Abstract] [Full Text] [Related]
6. Dyschondrosteosis (mesomelic dwarfism)--a family study.
Carter AR; Currey HL
Br J Radiol; 1974 Oct; 47(562):634-40. PubMed ID: 4433973
[No Abstract] [Full Text] [Related]
7. [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. PubMed ID: 5626375
[No Abstract] [Full Text] [Related]
8. Hypochondroplasia. A report of five kindreds.
Beals RK
J Bone Joint Surg Am; 1969 Jun; 51(4):728-36. PubMed ID: 5783850
[No Abstract] [Full Text] [Related]
9. Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type.
Flöttmann R; Wagner J; Kobus K; Curry CJ; Savarirayan R; Nishimura G; Yasui N; Spranger J; Van Esch H; Lyons MJ; DuPont BR; Dwivedi A; Klopocki E; Horn D; Mundlos S; Spielmann M
J Med Genet; 2015 Jul; 52(7):476-83. PubMed ID: 26032025
[TBL] [Abstract][Full Text] [Related]
10. Mesomelic dwarfism of the hypoplastic ulna, fibula, mandible type.
Langer LO
Radiology; 1967 Oct; 89(4):654-60. PubMed ID: 6059604
[No Abstract] [Full Text] [Related]
11. Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?
Petrella R; Ludman MD; Rabinowitz JG; Gilbert F; Hirschhorn K
Am J Med Genet; 1990 Sep; 37(1):10-4. PubMed ID: 2240023
[TBL] [Abstract][Full Text] [Related]
12. Dominant mesomelic dwarfism of the hypoplastic tibia, radius type.
Leroy JG; De Vos J; Timmermans J
Clin Genet; 1975 Apr; 7(4):280-6. PubMed ID: 1126050
[TBL] [Abstract][Full Text] [Related]
13. Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
Kantaputra PN; Gorlin RJ; Langer LO
Am J Med Genet; 1992 Dec; 44(6):730-7. PubMed ID: 1481840
[TBL] [Abstract][Full Text] [Related]
14. Congenital fusion of bones: radiology, embryology and pathogenesis.
McCredie J
Clin Radiol; 1975 Jan; 26(1):47-51. PubMed ID: 1122695
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 12597288
[TBL] [Abstract][Full Text] [Related]
16. Radiographic patterns of dyschondrosteosis. (Leri-Weill disease).
Hoeffel JC; Brauer B; Jimenez J; Hoeffel F
Radiol Clin Biol; 1973; 42(5):366-72. PubMed ID: 4745065
[No Abstract] [Full Text] [Related]
17. Familial congenital bowing of the tibia with pseudarthrosis and pectus excavatum: report of a kindred.
Beals RK; Fraser W
J Bone Joint Surg Am; 1976 Jun; 58(4):545-8. PubMed ID: 1270474
[No Abstract] [Full Text] [Related]
18. Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasias.
Fryns JP; Hofkens G; Fabry G; van den Berghe H
Clin Genet; 1988 Jan; 33(1):57-9. PubMed ID: 3342548
[TBL] [Abstract][Full Text] [Related]
19. The radiological diagnosis of the fetal-face (= Robinow) syndrome (mesomelic dwarfism and small genitalia). Report of 3 cases.
Giedion A; Battaglia GF; Bellini F; Fanconi G
Helv Paediatr Acta; 1976 Jan; 30(4-5):409-23. PubMed ID: 1245439
[TBL] [Abstract][Full Text] [Related]
20. Mesomelic dwarfism as the homozygous expression of dyschondrosteosis.
Espiritu C; Chen H; Woolley PV
Am J Dis Child; 1975 Mar; 129(3):375-7. PubMed ID: 1121969
[No Abstract] [Full Text] [Related]
[Next] [New Search]