96 related articles for article (PubMed ID: 3934623)
1. Dominant CHARGE association.
Mitchell JA; Giangiacomo J; Hefner MA; Thelin JW; Pickens JM
Ophthalmic Paediatr Genet; 1985 Aug; 6(1-2):271-6. PubMed ID: 3934623
[TBL] [Abstract][Full Text] [Related]
2. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
Stoll C; Terzic J; Fischbach M
Genet Couns; 1999; 10(4):337-43. PubMed ID: 10631920
[TBL] [Abstract][Full Text] [Related]
3. Dominant inheritance of bifid nose.
Anyane-Yeboa K; Raifman MA; Berant M; Frogel MP; Travers H
Am J Med Genet; 1984 Mar; 17(3):561-3. PubMed ID: 6711607
[TBL] [Abstract][Full Text] [Related]
4. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
Temtamy SA; Salam MA; Aboul-Ezz EH; Hussein HA; Helmy SA; Shalash BA
Clin Dysmorphol; 1996 Jul; 5(3):231-40. PubMed ID: 8818452
[TBL] [Abstract][Full Text] [Related]
5. Ruvalcaba syndrome: autosomal dominant inheritance.
Sugio Y; Kajii T
Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
[TBL] [Abstract][Full Text] [Related]
6. Dominant inheritance of holoprosencephaly.
Cantú JM; Fragoso R; Garcia-Cruz D; Sánchez-Corona J
Birth Defects Orig Artic Ser; 1978; 14(6B):215-20. PubMed ID: 728563
[No Abstract] [Full Text] [Related]
7. Re-evaluation of new X-linked syndrome for evidence of CHARGE syndrome or association.
Abruzzo MA; Erickson RP
Am J Med Genet; 1989 Nov; 34(3):397-400. PubMed ID: 2596527
[TBL] [Abstract][Full Text] [Related]
8. Typical ocular coloboma affects three generations in one family.
Hayasaka S; Furuse N; Noda S; Setogawa T
Ann Ophthalmol; 1992 Jun; 24(6):209-12. PubMed ID: 1444080
[TBL] [Abstract][Full Text] [Related]
9. Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.
Halal F; Homsy M; Perreault G
Am J Med Genet; 1984 Apr; 17(4):753-62. PubMed ID: 6426304
[TBL] [Abstract][Full Text] [Related]
10. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
Sadler LS; Robinson LK
Am J Med Genet; 1993 Aug; 47(1):65-8. PubMed ID: 8368255
[TBL] [Abstract][Full Text] [Related]
11. The CHARGE association in a newborn infant.
Akisü M; Ozkinay F; Ozyürek R; Küçüktaş A; Kültürsay N
Turk J Pediatr; 1998; 40(2):283-7. PubMed ID: 9714686
[TBL] [Abstract][Full Text] [Related]
12. New autosomal dominant branchio-oculo-facial syndrome.
Fujimoto A; Lipson M; Lacro RV; Shinno NW; Boelter WD; Jones KL; Wilson MG
Am J Med Genet; 1987 Aug; 27(4):943-51. PubMed ID: 3321995
[TBL] [Abstract][Full Text] [Related]
13. Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder.
Nöthen MM; Knöpfle G; Födisch HJ; Zerres K
Am J Med Genet; 1993 Jun; 46(4):467-70. PubMed ID: 8357025
[TBL] [Abstract][Full Text] [Related]
14. A distinct syndrome of familial cleft lip and palate with prominent eyes and characteristic facies in two unrelated families.
Kumar D; Garcia-Minaur S; Quarrell OW; Landa G; Garaizar C
Clin Dysmorphol; 1996 Oct; 5(4):295-301. PubMed ID: 8905193
[TBL] [Abstract][Full Text] [Related]
15. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
Brooks SS; Wisniewski K; Brown WT
Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
[TBL] [Abstract][Full Text] [Related]
16. Kabuki make-up syndrome and hearing impairment.
Say B; McCutcheon L; Todd C; Hough JV
Clin Dysmorphol; 1993 Jan; 2(1):68-70. PubMed ID: 8298741
[TBL] [Abstract][Full Text] [Related]
17. Dominant inheritance of microcephaly, short stature and congenital dislocation of the hips.
Newbury-Ecob RA; Young ID
Clin Dysmorphol; 1993 Jan; 2(1):34-8. PubMed ID: 8298736
[TBL] [Abstract][Full Text] [Related]
18. The syndrome of anosmia with hypogonadotropic hypogonadism: a genetic study of 18 new families and a review.
White BJ; Rogol AD; Brown KS; Lieblich JM; Rosen SW
Am J Med Genet; 1983 Jul; 15(3):417-35. PubMed ID: 6881209
[TBL] [Abstract][Full Text] [Related]
19. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH
Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066
[TBL] [Abstract][Full Text] [Related]
20. [Short stature, mental retardation, type I preaxial polydactyly with colobomatous abnormalities: a new syndrome].
Pfeiffer RA; Mayer U
Klin Monbl Augenheilkd; 1987 Dec; 191(6):473-7. PubMed ID: 3441111
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
