155 related articles for article (PubMed ID: 3377005)
1. A new autosomal recessive lethal chondrodystrophy with congenital hydrops.
Greenberg CR; Rimoin DL; Gruber HE; DeSa DJ; Reed M; Lachman RS
Am J Med Genet; 1988 Mar; 29(3):623-32. PubMed ID: 3377005
[TBL] [Abstract][Full Text] [Related]
2. Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder.
Chitayat D; Gruber H; Mullen BJ; Pauzner D; Costa T; Lachman R; Rimoin DL
Am J Med Genet; 1993 Aug; 47(2):272-7. PubMed ID: 8213919
[TBL] [Abstract][Full Text] [Related]
3. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
Borochowitz Z; Langer LO; Gruber HE; Lachman R; Katznelson MB; Rimoin DL
Am J Med Genet; 1993 Feb; 45(3):320-6. PubMed ID: 8434618
[TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive omodysplasia.
Stoll C; Pennerath A; Poirat P
Ann Genet; 1995; 38(2):97-101. PubMed ID: 7486832
[TBL] [Abstract][Full Text] [Related]
5. Greenberg dysplasia (hydrops-ectopic calcification-moth-eaten skeletal dysplasia): prenatal ultrasound diagnosis and review of literature.
Trajkovski Z; Vrcakovski M; Saveski J; Gucev ZS
Am J Med Genet; 2002 Sep; 111(4):415-9. PubMed ID: 12210303
[TBL] [Abstract][Full Text] [Related]
6. A new category of lethal short-limbed dwarfism.
Knowles S; Winter R; Rimoin D
Am J Med Genet; 1986 Sep; 25(1):41-6. PubMed ID: 3799722
[TBL] [Abstract][Full Text] [Related]
7. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
Franceschini P; Testa A; Bogetti G; Girardo E; Guala A; Lopez-Bell G; Buzio G; Ferrario E; Piccato E
Am J Med Genet; 1992 Jan; 42(1):112-6. PubMed ID: 1308349
[TBL] [Abstract][Full Text] [Related]
8. A new lethal autosomal recessive skeletal dysplasia with associated dysmorphic features.
Morton JE; Kilby MD; Rushton I
Clin Dysmorphol; 1998 Apr; 7(2):109-14. PubMed ID: 9571280
[TBL] [Abstract][Full Text] [Related]
9. Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity.
Aleck KA; Grix A; Clericuzio C; Kaplan P; Adomian GE; Lachman R; Rimoin DL
Am J Med Genet; 1987 Jun; 27(2):295-312. PubMed ID: 3605216
[TBL] [Abstract][Full Text] [Related]
10. A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasia.
Borochowitz Z; Jones KL; Silbey R; Adomian G; Lachman R; Rimoin DL
Am J Med Genet; 1986 Sep; 25(1):47-59. PubMed ID: 3799723
[TBL] [Abstract][Full Text] [Related]
11. Skeletal dysplasias with gracile bones: three new cases, including two offspring of a mother with a dwarfing condition.
Costa T; Azouz EM; Fitzpatrick J; Kamel-Reid S; Smith CR; Silver MM
Am J Med Genet; 1998 Mar; 76(2):125-32. PubMed ID: 9511974
[TBL] [Abstract][Full Text] [Related]
12. Spondyloepimetaphyseal dysplasia (SEMD) Shohat type.
Figuera LE; Ramírez-Dueñas ML; Gallegos-Arreola MP; Cantú JM
Am J Med Genet; 1994 Jul; 51(3):213-5. PubMed ID: 8074146
[TBL] [Abstract][Full Text] [Related]
13. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
Janssen HC; Schaap C; Vandevijver N; Moerman P; de Die-Smulders CE; Fryns JP
J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
[TBL] [Abstract][Full Text] [Related]
14. Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant.
Connor JM; Connor RA; Sweet EM; Gibson AA; Patrick WJ; McNay MB; Redford DH
Am J Med Genet; 1985 Oct; 22(2):243-53. PubMed ID: 3901754
[TBL] [Abstract][Full Text] [Related]
15. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
Miny P; Lenz W
Am J Med Genet; 1985 Jun; 21(2):317-24. PubMed ID: 4014313
[TBL] [Abstract][Full Text] [Related]
16. Familial Blomstrand chondrodysplasia with advanced skeletal maturation: further delineation.
Loshkajian A; Roume J; Stanescu V; Delezoide AL; Stampf F; Maroteaux P
Am J Med Genet; 1997 Aug; 71(3):283-8. PubMed ID: 9268097
[TBL] [Abstract][Full Text] [Related]
17. [Prenatal sonographic diagnosis of a case of Desbuquois familial osseous dysplasia].
Grischke EM; Tröger J; Schroeder-Kurth T; Schmidt W
Z Geburtshilfe Perinatol; 1989; 193(4):195-7. PubMed ID: 2678787
[TBL] [Abstract][Full Text] [Related]
18. Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.
Opitz JM; Spranger JW; Stöss HR; Pesch HJ; Azadeh B
Am J Med Genet; 1987 Mar; 26(3):583-90. PubMed ID: 3565474
[TBL] [Abstract][Full Text] [Related]
19. Fibrochondrogenesis.
Kulkarni ML; Matadh PS; Praveen Prabhu SP; Kulkarni PM
Indian J Pediatr; 2005 Apr; 72(4):355-7. PubMed ID: 15876767
[TBL] [Abstract][Full Text] [Related]
20. Schneckenbecken dysplasia in fetus: report of four cases.
Lahmar-Boufaroua A; Yacoubi MT; Belaid L; Delezoide AL
Fetal Diagn Ther; 2009; 25(2):216-9. PubMed ID: 19407457
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]