216 related articles for article (PubMed ID: 8213920)
1. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome.
Richieri-Costa A; Guion-Almeida ML; Cohen MM
Am J Med Genet; 1993 Aug; 47(2):278-80. PubMed ID: 8213920
[TBL] [Abstract][Full Text] [Related]
2. Previously undescribed spondyloepiphyseal dysplasia associated with craniosynostosis, cataracts, cleft palate, and mental retardation: report of four sibs.
Nishimura G; Fukushima Y; Aihara T; Ohashi H; Nishimoto H; Nishimura J
Am J Med Genet; 1998 Apr; 77(1):1-7. PubMed ID: 9557884
[TBL] [Abstract][Full Text] [Related]
3. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents.
Richieri-Costa A; Pirolo Júnior L; Cohen MM
Am J Med Genet; 1993 Aug; 47(2):281-3. PubMed ID: 8213921
[TBL] [Abstract][Full Text] [Related]
4. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ
Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. [Spondylo-epiphyseal dysplasia associated with craniosynostosis, cleft palate and mental retardation. A case report].
Herrera-Martínez AD; Estrada-Corona P
Invest Clin; 2010 Dec; 51(4):553-60. PubMed ID: 21365879
[TBL] [Abstract][Full Text] [Related]
8. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Craniosynostosis and lid anomalies: report of a girl with Michels syndrome.
Cunniff C; Jones KL
Am J Med Genet; 1990 Sep; 37(1):28-30. PubMed ID: 2240039
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Craniomicromelic syndrome: a newly recognized lethal condition with craniosynostosis, distinct facial anomalies, short limbs, and intrauterine growth retardation.
Barr M; Heidelberger KP; Comstock CH
Am J Med Genet; 1995 Sep; 58(4):348-52. PubMed ID: 8533844
[TBL] [Abstract][Full Text] [Related]
13. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause.
Richieri-Costa A; Guion-Almeida ML
Am J Med Genet; 1993 Oct; 47(5):702-6. PubMed ID: 8266999
[TBL] [Abstract][Full Text] [Related]
14. New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.
Borochowitz Z; Pavone L; Mazor G; Rizzo R; Dar H
Am J Med Genet; 1992 Jul; 43(4):678-85. PubMed ID: 1621757
[TBL] [Abstract][Full Text] [Related]
15. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
da-Silva EO
Am J Med Genet; 1988 Apr; 29(4):837-43. PubMed ID: 3400727
[TBL] [Abstract][Full Text] [Related]
16. Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defect.
Buttiens M; Fryns JP
Am J Med Genet; 1987 Jul; 27(3):651-60. PubMed ID: 3631136
[TBL] [Abstract][Full Text] [Related]
17. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
Bonioli E; Palmieri A; Bertola A; Bellini C
Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
[TBL] [Abstract][Full Text] [Related]
18. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
Richieri-Costa A; Guion-Almeida ML; Lauris JR; Ferreira DM
Am J Med Genet; 1994 Jan; 49(2):224-8. PubMed ID: 8116673
[TBL] [Abstract][Full Text] [Related]
19. C syndrome with apparently normal development.
Stratton RF; Sykes NJ; Hassler TW
Am J Med Genet; 1990 Dec; 37(4):460-2. PubMed ID: 2260587
[TBL] [Abstract][Full Text] [Related]
20. Cerebro-reno-digital syndrome in two sibs.
Piantanida M; Tiberti A; Plebani A; Martelli P; Danesino C
Am J Med Genet; 1993 Sep; 47(3):420-2. PubMed ID: 8135292
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]