140 related articles for article (PubMed ID: 8723088)
1. Metaphyseal peg in geroderma osteodysplasticum: a new genetic bone marker and a specific finding?
Eich GF; Steinmann B; Hodler J; Exner GU; Giedion A
Am J Med Genet; 1996 May; 63(1):62-7. PubMed ID: 8723088
[TBL] [Abstract][Full Text] [Related]
2. Metaphyseal dysplasia of Braun-Tinschert type: report of a Japanese girl.
Takata S; Nishimura G; Ikegawa S; Kuroda Y; Nishino M; Matsui Y; Yasui N
Am J Med Genet A; 2006 Jun; 140(11):1234-7. PubMed ID: 16691581
[TBL] [Abstract][Full Text] [Related]
3. Unusual bone dysplasia featuring severe platyspondyly and vertebral "coronal cleft" in infancy, and changes of metaphyseal chondrodysplasia in childhood.
Currarino G
Pediatr Radiol; 1986; 16(5):433-6. PubMed ID: 3748653
[TBL] [Abstract][Full Text] [Related]
4. Bilateral radial ray hypoplasia with multiple epiphyseal dysplasia.
Eddy MC; Steiner RD; McAlister WH; Whyte MP
Am J Med Genet; 1998 May; 77(3):182-7. PubMed ID: 9605584
[TBL] [Abstract][Full Text] [Related]
5. Dutch variant of Bellini metaphyseal dysplasia: report of two siblings.
Kozlowski K; Meradji M; Beemer FA
Australas Radiol; 1995 Aug; 39(3):282-6. PubMed ID: 7487766
[TBL] [Abstract][Full Text] [Related]
6. [Gollop-Wolfgang complex: tibial hemimelia associated with bifid femur and hypodactyly].
Göblyös P; Czeizel E
Orv Hetil; 1995 Mar; 136(11):609-11. PubMed ID: 7700619
[No Abstract] [Full Text] [Related]
7. Aplasia of the tibia with bifurcation of the femur and ectrodactyly: evidence for an autosomal recessive type.
Kohn G; el Shawwa R; Grunebaum M
Am J Med Genet; 1989 Jun; 33(2):172-5. PubMed ID: 2764026
[TBL] [Abstract][Full Text] [Related]
8. Atelosteogenesis.
Maroteaux P; Spranger J; Stanescu V; Le Marec B; Pfeiffer RA; Beighton P; Mattei JF
Am J Med Genet; 1982 Sep; 13(1):15-25. PubMed ID: 7137218
[TBL] [Abstract][Full Text] [Related]
9. [The FF complex: a rare congenital malformation].
Smilari P; Pavone V; Saporito A; Parisi M; Carpinato C; Sorge G
Pediatr Med Chir; 1997; 19(3):215-7. PubMed ID: 9340614
[No Abstract] [Full Text] [Related]
10. Stüve-Wiedemann syndrome: update and historical footnote.
Wiedemann HR; Stüve A
Am J Med Genet; 1996 May; 63(1):12-6. PubMed ID: 8723080
[TBL] [Abstract][Full Text] [Related]
11. Fibrochondrogenesis: radiologic and histologic studies.
Eteson DJ; Adomian GE; Ornoy A; Koide T; Sugiura Y; Calabro A; Lungarotti S; Mastroiacovo P; Lachman RS; Rimoin DL
Am J Med Genet; 1984 Oct; 19(2):277-90. PubMed ID: 6507479
[TBL] [Abstract][Full Text] [Related]
12. Proximal focal femoral deficiency.
Mehrotra G; Bhargava SK; Shiv VK; Taneja K
Indian Pediatr; 1993 Feb; 30(2):241-5. PubMed ID: 8375888
[No Abstract] [Full Text] [Related]
13. Micromelic dwarfism--humerus, femur, tibia type. Report of a case.
Baxova A; Kozlowski K; Netriova I
Pediatr Radiol; 1993; 23(6):446-9. PubMed ID: 8255648
[TBL] [Abstract][Full Text] [Related]
14. Pyle metaphyseal dysplasia.
Gupta N; Kabra M; Das CJ; Gupta AK
Indian Pediatr; 2008 Apr; 45(4):323-5. PubMed ID: 18451455
[TBL] [Abstract][Full Text] [Related]
15. Desbuquois dysplasia, a reevaluation with abnormal and "normal" hands: radiographic manifestations.
Faivre L; Cormier-Daire V; Eliott AM; Field F; Munnich A; Maroteaux P; Le Merrer M; Lachman R
Am J Med Genet A; 2004 Jan; 124A(1):48-53. PubMed ID: 14679586
[TBL] [Abstract][Full Text] [Related]
16. Spondylo-epi-metaphyseal dysplasia with normal stature: a case followed from infancy to skeletal maturity.
Nakamura S; Haga N; Shimode M; Taniguchi K; Ikegawa S; Iwaya T
Clin Dysmorphol; 1999 Jul; 8(3):189-92. PubMed ID: 10457852
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of Gollop-Wolfgang complex.
Caforio L; Pagnotta G; Romiti A; Familiari A; Donati F; Bagolan P
Ultrasound Obstet Gynecol; 2015 Apr; 45(4):488-90. PubMed ID: 25302853
[No Abstract] [Full Text] [Related]
18. Diastrophic dysplasia: extreme variability within a sibship.
Hall BD
Am J Med Genet; 1996 May; 63(1):28-33. PubMed ID: 8723083
[TBL] [Abstract][Full Text] [Related]
19. Omodysplasia: an affected mother and son.
Venditti CP; Farmer J; Russell KL; Friedrich CA; Alter C; Canning D; Whitaker L; Mennuti MT; Driscoll DA; Zackai EH
Am J Med Genet; 2002 Aug; 111(2):169-77. PubMed ID: 12210345
[TBL] [Abstract][Full Text] [Related]
20. Campomelic syndrome.
Sehgal SK; Puri S; Wadhwa A; Pathak OP; Mohan M; Anand NK
Indian Pediatr; 1990 Jun; 27(6):619-22. PubMed ID: 2253999
[No Abstract] [Full Text] [Related]
[Next] [New Search]
