128 related articles for article (PubMed ID: 12002138)
1. Syndromic dystelephalangy.
Chrzanowska K; Kowalska A; Koziowski K
Clin Dysmorphol; 2002 Apr; 11(2):103-5. PubMed ID: 12002138
[TBL] [Abstract][Full Text] [Related]
2. [The Coffin-Siris syndrome. A new syndrome of mental retardation, hypo-aplasia of the nails and terminal phalanges of the 5th fingers and toes].
Mastroiacovo P; Salvaggio E; Parenti D
Minerva Pediatr; 1977 Mar; 29(11):773-8. PubMed ID: 875947
[No Abstract] [Full Text] [Related]
3. The Coffin-Siris syndrome.
Schinzel A
Acta Paediatr Scand; 1979 May; 68(3):449-52. PubMed ID: 155976
[TBL] [Abstract][Full Text] [Related]
4. Trichorhinophalangeal dysplasia (Giedion syndrome). A case report.
Kuna GB; Collipp PJ; Balsam D
Clin Pediatr (Phila); 1978 Jan; 17(1):96-8. PubMed ID: 618703
[TBL] [Abstract][Full Text] [Related]
5. The Coffin-Siris syndrome. A report of four cases and review of the literature.
Lucaya J; Garcia-Conesa JA; Bosch-Banyeras JM; Pons-Peradejordi G
Pediatr Radiol; 1981; 11(1):35-8. PubMed ID: 7019832
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Radiographic observations of pyknodysostosis. Report of a case.
Kawahara K; Nishikiori M; Imai K; Kishi K; Fujiki Y
Oral Surg Oral Med Oral Pathol; 1977 Sep; 44(3):476-82. PubMed ID: 269344
[TBL] [Abstract][Full Text] [Related]
8. Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome.
Hoffman HM; Bastian JF; Bird LM
Clin Dysmorphol; 2001 Jan; 10(1):1-8. PubMed ID: 11152140
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Cohen syndrome. Contribution to its clinical delineation].
Lapetina F; Piantoni G; Canino R; Teza F; Ferrarini D
Pediatr Med Chir; 1988; 10(2):217-21. PubMed ID: 3174485
[TBL] [Abstract][Full Text] [Related]
11. Abnormal distal phalanges and nails, deafness, mental retardation, and seizure disorder: a new familial syndrome.
Qazi QH; Nangia BS
J Pediatr; 1984 Mar; 104(3):391-4. PubMed ID: 6707793
[TBL] [Abstract][Full Text] [Related]
12. A patient with facial abnormality, imperforate anus, tetrapolyhypodactyly and meningocele: a variable manifestation of the polyoligodactyly/imperforate anus/vertebral anomalies syndrome.
Sener RN
Pediatr Radiol; 1994; 24(8):598-9. PubMed ID: 7724288
[TBL] [Abstract][Full Text] [Related]
13. SED-brachydactyly and distinctive speech: report of two new cases.
García-Cruz D; Zafra de la Rosa GF; Sánchez-Corona J; Nazará Z; López-Cardona MG; García-Ortiz JE; Corona-Rivera JR; Cantú JM
Genet Couns; 2007; 18(1):85-97. PubMed ID: 17515304
[TBL] [Abstract][Full Text] [Related]
14. [Feingold syndrome].
Alessandri JL; Graber D; Tiran-Rajaofera I; Montbrun A; Pilorget H; Samperiz S; Attali T; de Napoli-Cocci S
Arch Pediatr; 2000 Jun; 7(6):637-40. PubMed ID: 10911531
[TBL] [Abstract][Full Text] [Related]
15. Diphenylhydantoin teratogenicity in man.
Yang TS; Chi CC; Tsai CJ; Chang MJ
Obstet Gynecol; 1978 Dec; 52(6):682-4. PubMed ID: 733136
[TBL] [Abstract][Full Text] [Related]
16. A new syndrome of broad terminal phalanges and facial abnormalities.
Keipert JA; Fitzgerald MG; Danks DM
Aust Paediatr J; 1973 Feb; 9(1):10-3. PubMed ID: 4708024
[No Abstract] [Full Text] [Related]
17. Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type.
Kantaputra PN; Gorlin RJ; Ukarapol N; Unachak K; Sudasna J
Am J Med Genet; 1999 May; 84(1):1-7. PubMed ID: 10213037
[TBL] [Abstract][Full Text] [Related]
18. Brachymorphism-onychodysplasia-dysphalangism syndrome.
Verloes A; Bonneau D; Guidi O; Berthier M; Oriot D; Van Maldergem L; Koulischer L
J Med Genet; 1993 Feb; 30(2):158-61. PubMed ID: 8445623
[TBL] [Abstract][Full Text] [Related]
19. Hereditary ulnar and fibular dimelia with peculiar facies. A case report.
Sandrow RE; Sullivan PD; Steel HH
J Bone Joint Surg Am; 1970 Mar; 52(2):367-70. PubMed ID: 4314818
[No Abstract] [Full Text] [Related]
20. Two sisters with growth failure, microcephaly, peculiar facies and apical dystrophy: the presentation of brachymorphism-onychodysplasia-dysphalangism syndrome?
Ounap K; Justus I; Lipping-Sitska M
Clin Dysmorphol; 1998 Jan; 7(1):45-50. PubMed ID: 9546830
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
