187 related articles for article (PubMed ID: 3425604)
1. Robin sequence and oligodactyly in mother and son--probably a further example of the postaxial acrofacial dysostosis syndrome.
Meinecke P; Wiedemann HR
Am J Med Genet; 1987 Aug; 27(4):953-7. PubMed ID: 3425604
[No Abstract] [Full Text] [Related]
2. Robin sequence and oligodactyly in mother and son.
Robinow M; Johnson GF; Apesos J
Am J Med Genet; 1986 Oct; 25(2):293-7. PubMed ID: 3777025
[TBL] [Abstract][Full Text] [Related]
3. The Genée-Wiedemann syndrome, an acrofacial dysostosis--further observation.
Opitz JM; Stickler GB
Am J Med Genet; 1987 Aug; 27(4):971-5. PubMed ID: 3425606
[No Abstract] [Full Text] [Related]
4. The Greig cephalopolysyndactyly syndrome in a Canadian family.
Chudley AE; Houston CS
Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
[No Abstract] [Full Text] [Related]
5. Postaxial acrofacial dysostosis syndrome.
Miller M; Fineman R; Smith DW
J Pediatr; 1979 Dec; 95(6):970-5. PubMed ID: 501501
[TBL] [Abstract][Full Text] [Related]
6. M--craniocarpotarsal dystrophy (whistling face syndrome) in two families.
Jorgenson RJ
Birth Defects Orig Artic Ser; 1974; 10(5):237-42. PubMed ID: 4220006
[No Abstract] [Full Text] [Related]
7. Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients.
Chrzanowska KH; Fryns JP; Krajewska-Walasek M; Wisniewski L; Van den Berghe H
Clin Genet; 1989 Feb; 35(2):157-60. PubMed ID: 2721025
[TBL] [Abstract][Full Text] [Related]
8. Nager acrofacial dysostosis: autosomal dominant inheritance in mild to moderately affected mother and lethally affected phocomelic son.
Hall BD
Am J Med Genet; 1989 Jul; 33(3):394-7. PubMed ID: 2801774
[TBL] [Abstract][Full Text] [Related]
9. Robin sequence with facial and digital anomalies in two half-brothers by the same mother.
Chitayat D; Meunier CM; Hodgkinson KA; Azouz ME
Am J Med Genet; 1991 Aug; 40(2):167-72. PubMed ID: 1897570
[TBL] [Abstract][Full Text] [Related]
10. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
[No Abstract] [Full Text] [Related]
11. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
Guttmacher AE
Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
[TBL] [Abstract][Full Text] [Related]
12. Postaxial acrofacial dysostosis (Miller) syndrome: a new case.
Vigneron J; Stricker M; Vert P; Rousselot JM; Levy M
J Med Genet; 1991 Sep; 28(9):636-8. PubMed ID: 1683410
[TBL] [Abstract][Full Text] [Related]
13. Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?
Stoll C; Kieny JR; Dott B; Alembik Y; Finck S
Am J Med Genet; 1992 Feb; 42(4):480-6. PubMed ID: 1376967
[TBL] [Abstract][Full Text] [Related]
14. Postaxial acrofacial dysostosis or Miller syndrome. A case report.
Barbuti D; Orazi C; Reale A; Paradisi C
Eur J Pediatr; 1989 Feb; 148(5):445-6. PubMed ID: 2920751
[TBL] [Abstract][Full Text] [Related]
15. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.
Richieri-Costa A; Pereira SC
Am J Med Genet; 1993 Oct; 47(5):707-9. PubMed ID: 8267000
[TBL] [Abstract][Full Text] [Related]
16. New lethal acrofacial dysostosis syndrome.
Fryns JP; Kleckowska A
Am J Med Genet; 1991 May; 39(2):223-4. PubMed ID: 1822088
[No Abstract] [Full Text] [Related]
17. Abnormal facies, cleft palate, and generalized dysostosis: a lethal X-linked syndrome.
André M; Vigneron J; Didier F
J Pediatr; 1981 May; 98(5):747-52. PubMed ID: 7229752
[TBL] [Abstract][Full Text] [Related]
18. Catel-Manzke syndrome: two new patients and a critical review of the literature.
Manzke H; Lehmann K; Klopocki E; Caliebe A
Eur J Med Genet; 2008; 51(5):452-65. PubMed ID: 18501694
[TBL] [Abstract][Full Text] [Related]
19. [Meyer-Schwickerath and Grüterich-Weyers syndrome].
Lukova NB; Snisarevskiĭ DA; Eroshevskiĭ BT
Vestn Oftalmol; 1978; (1):84-6. PubMed ID: 636166
[No Abstract] [Full Text] [Related]
20. Marshall syndrome.
Stratton RF; Lee B; Ramirez F
Am J Med Genet; 1991 Oct; 41(1):35-8. PubMed ID: 1951461
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]