160 related articles for article (PubMed ID: 8905197)
1. A syndrome of short stature, mental retardation, facial dysmorphism, short webbed neck, skin changes and congenital heart disease.
al-Gazali LI; Aziz SA; Salem F
Clin Dysmorphol; 1996 Oct; 5(4):321-7. PubMed ID: 8905197
[TBL] [Abstract][Full Text] [Related]
2. Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: new cases of "polyvalvular heart disease syndrome" or new association?
Edouard T; Prost-Squarcioni C; Dulac Y; Vaysse F; Cavé H; Saugier-Veber P; Bourrouillou G; Verloes A; Tauber M; Bieth E
Eur J Med Genet; 2010; 53(1):29-34. PubMed ID: 19932204
[TBL] [Abstract][Full Text] [Related]
3. Syndrome identification case report 100: unusual facies, cleft palate, short stature, and mental retardation.
Feingold M; Trainer J
J Clin Dysmorphol; 1983; 1(2):22-3. PubMed ID: 6580391
[No Abstract] [Full Text] [Related]
4. "A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities": Cohen syndrome with thrombocytopenia.
De Ravel TJ; Dillen K; Fryns JP
Genet Couns; 2002; 13(4):475-6. PubMed ID: 12558120
[No Abstract] [Full Text] [Related]
5. IQ and the somatic stigmata of Turner's syndrome.
Money J; Granoff D
Am J Ment Defic; 1965 Jul; 70(1):69-77. PubMed ID: 5830573
[No Abstract] [Full Text] [Related]
6. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.
Herrmann J; Pallister PD; Tiddy W; Opitz JM
Birth Defects Orig Artic Ser; 1975; 11(5):7-18. PubMed ID: 1218237
[No Abstract] [Full Text] [Related]
7. Macrocephaly, facial abnormalities, disproportionate tall stature, and mental retardation--a sib observation.
Bakker HD; Hennekam RC
Am J Med Genet; 1997 Jun; 70(3):312-4. PubMed ID: 9188672
[TBL] [Abstract][Full Text] [Related]
8. Apparently new syndrome of congenital cataracts, sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardation.
Gripp KW; Nicholson L; Scott CI
Am J Med Genet; 1996 Feb; 61(4):382-6. PubMed ID: 8834052
[TBL] [Abstract][Full Text] [Related]
9. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
Tsukahara M; Sugio Y
J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671
[TBL] [Abstract][Full Text] [Related]
10. [Pterygia-dysmorphic facies-short stature-mental retardation].
Tonoki H
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):545. PubMed ID: 11528885
[No Abstract] [Full Text] [Related]
11. Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
Mégarbané A; Choueiri R; Bleik J; Mezzina M; Caillaud C
J Med Genet; 1999 Aug; 36(8):637-40. PubMed ID: 10465117
[TBL] [Abstract][Full Text] [Related]
12. Does the cranio-cerebello-cardiac syndrome (3C syndrome) include abdominal malformations?
Mégarbané A; Haddad J
Clin Dysmorphol; 1999 Oct; 8(4):305-7. PubMed ID: 10532184
[TBL] [Abstract][Full Text] [Related]
13. Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings.
Przedborski S; Ferster A; Goldman S; Wolter R; Song M; Tonnesen T; Pollitt RJ; Vamos E
Am J Med Genet; 1990 Apr; 35(4):566-73. PubMed ID: 2333887
[TBL] [Abstract][Full Text] [Related]
14. A boy with choanal atresia and cardiac defect: Burn-McKeown syndrome?
Toriello HV; Higgins JV
Clin Dysmorphol; 1999 Apr; 8(2):143-5. PubMed ID: 10319205
[TBL] [Abstract][Full Text] [Related]
15. Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome.
Mori PG; Priolo M; Lerone M; Pasino M; Caroli F; Cusano R; Seri M; Silengo MC
Am J Med Genet; 1999 Nov; 87(1):36-9. PubMed ID: 10528244
[TBL] [Abstract][Full Text] [Related]
16. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
[TBL] [Abstract][Full Text] [Related]
17. [Young-Simpson syndrome].
Masuno M
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):837-8. PubMed ID: 11529049
[No Abstract] [Full Text] [Related]
18. Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome.
Schnur RE; Greenbaum BH; Heymann WR; Christensen K; Buck AS; Reid CS
Am J Med Genet; 1997 Oct; 72(1):24-9. PubMed ID: 9295069
[TBL] [Abstract][Full Text] [Related]
19. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
Yüksel A; Seven M; Deviren A; Söylemez MA; Hacihanefioğlu S; Ulutin T; Cenani A
Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
[TBL] [Abstract][Full Text] [Related]
20. Siblings with glaucoma, mental retardation and short stature.
AlKaissi A; Hammou A; Ghachem MB; Nacib MN; Chehida FB; Karoui H; Baraitser M
Clin Dysmorphol; 2003 Jul; 12(3):191-4. PubMed ID: 14564159
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
