139 related articles for article (PubMed ID: 7593576)
1. Craniofacial conodysplasia.
Beals RK; Piatt JH; Zonana J
J Pediatr Orthop; 1995; 15(5):633-6. PubMed ID: 7593576
[TBL] [Abstract][Full Text] [Related]
2. Otopalatodigital syndrome type II.
Holder SE; Winter RM
J Med Genet; 1993 Apr; 30(4):310-3. PubMed ID: 8487277
[No Abstract] [Full Text] [Related]
3. A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).
Merlob P; Grünebaum M; Reisner SH
Acta Paediatr Scand; 1981 Mar; 70(2):275-7. PubMed ID: 6263040
[TBL] [Abstract][Full Text] [Related]
4. [Cranial metaphysial dysplasia (Jackson) (author's transl)].
Wemmer U; Böttger E
Rofo; 1978 Jan; 128(1):66-9. PubMed ID: 146664
[TBL] [Abstract][Full Text] [Related]
5. Cone-shaped epiphyses in the distal phalanges. Case report of a child with anorchia.
Saldino RM; Marshall S; Taybi H
Radiol Clin Biol; 1972; 41(6):449-52. PubMed ID: 4404981
[No Abstract] [Full Text] [Related]
6. A new skeletal dysplasia syndrome with dwarfism, craniofacial anomalies, and unique radiographic findings.
Jones KL; Jones KL; Miller K
Am J Med Genet; 1986 Mar; 23(3):751-7. PubMed ID: 2420178
[TBL] [Abstract][Full Text] [Related]
7. Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.
Ausems MG; Ippel PF; Renardel de Lavalette PA
Clin Dysmorphol; 1994 Jan; 3(1):21-30. PubMed ID: 8205322
[TBL] [Abstract][Full Text] [Related]
8. [A case of congenital hypodactyly of the hand and foot].
Mamedov AG; Seidov MM
Ortop Travmatol Protez; 1991 Apr; (4):51-2. PubMed ID: 1754179
[No Abstract] [Full Text] [Related]
9. Neonatal hyperthyroidism with accelerated skeletal maturation, craniosynostosis, and brachydactyly.
Riggs W; Wilroy RS; Etteldorf JN
Radiology; 1972 Dec; 105(3):621-5. PubMed ID: 4642468
[No Abstract] [Full Text] [Related]
10. Severe presentation of Peters'-Plus syndrome.
Lacombe D; Llanas B; Chateil JF; Sarrazin E; Carles D; Battin J
Clin Dysmorphol; 1994 Oct; 3(4):358-60. PubMed ID: 7894743
[No Abstract] [Full Text] [Related]
11. Terminal osseous dysplasia with pigmentary defects (TODPD) in a Turkish girl with new skin findings.
Azakli H; Akkaya AD; Aygün MS; Demirkesen C; Eraslan S; Kayserili H
Am J Med Genet A; 2019 Jan; 179(1):123-129. PubMed ID: 30561107
[TBL] [Abstract][Full Text] [Related]
12. Acrocapitofemoral dysplasia: an autosomal recessive skeletal dysplasia with cone shaped epiphyses in the hands and hips.
Mortier GR; Kramer PP; Giedion A; Beemer FA
J Med Genet; 2003 Mar; 40(3):201-7. PubMed ID: 12624140
[No Abstract] [Full Text] [Related]
13. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
Gollop TR; Fontes LR
Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752
[TBL] [Abstract][Full Text] [Related]
14. A new form of spondyloperipheral dysplasia with facial dysmorphism, flattened vertebrae, hypoplastic pelvis, brachydactyly and soft tissue syndactyly.
Kitoh H; Lachman RS
Pediatr Radiol; 2001 Jan; 31(1):23-6. PubMed ID: 11200993
[TBL] [Abstract][Full Text] [Related]
15. [Brachydactyly type A4 (brachymesophalangia II and V, Temtamy type). A rare type of brachydactyly].
Reichenbach H; Hörmann D; Theile H
Kinderarztl Prax; 1993 Mar; 61(2):59-62. PubMed ID: 8510402
[TBL] [Abstract][Full Text] [Related]
16. [The delta phalanx].
Csorba E
Magy Traumatol Orthop Helyreallito Seb; 1987; 30(2):103-9. PubMed ID: 2884354
[No Abstract] [Full Text] [Related]
17. Bone and joint manifestations of Rieger's syndrome: a report of a family.
Koshino T; Konno T; Ohzeki T
J Pediatr Orthop; 1989; 9(2):224-30. PubMed ID: 2494224
[TBL] [Abstract][Full Text] [Related]
18. [The cone-shaped epiphyses of the hands and feet (peripheral dysostosis].
LIESS G
Fortschr Geb Rontgenstr; 1954 Aug; 81(2):173-81. PubMed ID: 13200642
[No Abstract] [Full Text] [Related]
19. Hypotrichosis, bulbous nose, and cone-shaped epiphyses in an 8-year-old girl. Trichorhinophalangeal syndrome type I.
Sayed CJ; Matheis P; Morrell DS
Pediatr Dermatol; 2008; 25(5):557-8. PubMed ID: 18950401
[No Abstract] [Full Text] [Related]
20. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
Henkel KE; Pfeiffer RA; Stöss H
Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
[No Abstract] [Full Text] [Related]
[Next] [New Search]