278 related articles for article (PubMed ID: 7710257)
1. Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?
Stoll C; Alembik Y; Dott B
Ann Genet; 1994; 37(4):207-9. PubMed ID: 7710257
[TBL] [Abstract][Full Text] [Related]
2. The Okihiro syndrome of Duane anomaly, radial ray abnormalities, and deafness.
Hayes A; Costa T; Polomeno RC
Am J Med Genet; 1985 Oct; 22(2):273-80. PubMed ID: 4050857
[TBL] [Abstract][Full Text] [Related]
3. SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders.
Kohlhase J; Chitayat D; Kotzot D; Ceylaner S; Froster UG; Fuchs S; Montgomery T; Rösler B
Hum Mutat; 2005 Sep; 26(3):176-83. PubMed ID: 16086360
[TBL] [Abstract][Full Text] [Related]
4. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
Bindewald B; Ulmer H; Müller U
Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348
[TBL] [Abstract][Full Text] [Related]
5. Complex congenital heart disease, microcephaly, pheochromocytoma and neurofibromatosis type I in a girl born from consanguineous parents.
Stoll C; Alembik Y; Dott B
Genet Couns; 1995; 6(3):217-20. PubMed ID: 8588849
[TBL] [Abstract][Full Text] [Related]
6. [Cardiac symptoms in 2 patients with Seckel syndrome].
Rappen U; von Brenndorff AI
Monatsschr Kinderheilkd; 1993 Jul; 141(7):584-6. PubMed ID: 8413337
[TBL] [Abstract][Full Text] [Related]
7. A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents.
Stoll C; Alembik Y; Lutz P
Genet Couns; 1994; 5(2):161-5. PubMed ID: 7917125
[TBL] [Abstract][Full Text] [Related]
8. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
Verloes A; Dodinval P; Beco L; Bonnivert J; Lambotte C
Am J Med Genet; 1990 Sep; 37(1):119-23. PubMed ID: 2240028
[TBL] [Abstract][Full Text] [Related]
9. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH
Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045
[TBL] [Abstract][Full Text] [Related]
10. Apparently new MCA/MR syndrome in sibs with cleft lip and palate and other facial, eye, heart, and intestinal anomalies.
Kapur S; Toriello HV
Am J Med Genet; 1991 Dec; 41(4):423-5. PubMed ID: 1776630
[TBL] [Abstract][Full Text] [Related]
11. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
Malpuech G; Demeocq F; Palcoux JB; Vanlieferinghen P
Am J Med Genet; 1983 Dec; 16(4):475-80. PubMed ID: 6660246
[TBL] [Abstract][Full Text] [Related]
12. Association of ocular, cervical, and cardiac malformations.
Awan KJ
Ann Ophthalmol; 1977 Aug; 9(8):1001-11. PubMed ID: 409324
[TBL] [Abstract][Full Text] [Related]
13. Cataract, hypertrichosis, and mental retardation (CAHMR): a new autosomal recessive syndrome.
Temtamy SA; Sinbawy AH
Am J Med Genet; 1991 Dec; 41(4):432-3. PubMed ID: 1776632
[TBL] [Abstract][Full Text] [Related]
14. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
Kotzot D; Richter K; Gierth-Fiebig K
Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
[TBL] [Abstract][Full Text] [Related]
15. Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphy.
Stoll C; Finck S; Janser B; Printz M; Lutz P
Genet Couns; 1992; 3(1):41-7. PubMed ID: 1590980
[TBL] [Abstract][Full Text] [Related]
16. Opitz trigonocephaly syndrome.
Haaf T; Hofmann R; Schmid M
Am J Med Genet; 1991 Sep; 40(4):444-6. PubMed ID: 1746609
[TBL] [Abstract][Full Text] [Related]
17. Mutchinick syndrome in a Japanese girl.
Tonoki H; Hattori T; Kamoshida H; Ohta Y; Niikawa N
Am J Med Genet; 1999 Mar; 83(2):96-9. PubMed ID: 10190479
[TBL] [Abstract][Full Text] [Related]
18. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects.
Zlotogora J; Glick B
Am J Med Genet; 1993 Aug; 47(1):89-90. PubMed ID: 8368260
[TBL] [Abstract][Full Text] [Related]
19. Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22.
Cullen P; Rodgers CS; Callen DF; Connolly VM; Eyre H; Fells P; Gordon H; Winter RM; Thakker RV
Am J Med Genet; 1993 Nov; 47(6):925-30. PubMed ID: 8279492
[TBL] [Abstract][Full Text] [Related]
20. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
Angle B; Hersh JH
Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]