84 related articles for article (PubMed ID: 9188672)
1. 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]
2. Costello syndrome.
Der Kaloustian VM; Moroz B; McIntosh N; Watters AK; Blaichman S
Am J Med Genet; 1991 Oct; 41(1):69-73. PubMed ID: 1951465
[TBL] [Abstract][Full Text] [Related]
3. 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]
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. Smith-Fineman-Myers syndrome in two brothers.
Adès LC; Kerr B; Turner G; Wise G
Am J Med Genet; 1991 Sep; 40(4):467-70. PubMed ID: 1684092
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. [Dento-maxillo-facial anomalies in the KBG syndrome].
Tollaro I; v Bassarelli ; Calzolari C; Franchini F; Giovannucci Uzielli ML; Vieri PL
Minerva Stomatol; 1984; 33(3):437-46. PubMed ID: 6589471
[No Abstract] [Full Text] [Related]
9. Endocardial fibroelastosis, neurologic dysfunction and unusual facial appearance in two brothers, coincidentally associated with dominantly inherited macrocephaly.
Jennings MT; Hall JG; Kukolich M
Am J Med Genet; 1980; 5(3):271-6. PubMed ID: 6105824
[TBL] [Abstract][Full Text] [Related]
10. Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?
Ioan DM; Fryns JP
Genet Couns; 2002; 13(3):353-6. PubMed ID: 12416645
[TBL] [Abstract][Full Text] [Related]
11. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
Bibas Bonet H; Fontenla M; Fauze R; G de Pinat I
Rev Neurol; 2001 Apr 16-30; 32(8):746-50. PubMed ID: 11391511
[TBL] [Abstract][Full Text] [Related]
12. Kabuki syndrome: a review.
Adam MP; Hudgins L
Clin Genet; 2005 Mar; 67(3):209-19. PubMed ID: 15691356
[TBL] [Abstract][Full Text] [Related]
13. Kabuki syndrome: report of six Thai children and further phenotypic and genetic delineation.
Shotelersuk V; Punyashthiti R; Srivuthana S; Wacharasindhu S
Am J Med Genet; 2002 Jul; 110(4):384-90. PubMed ID: 12116214
[TBL] [Abstract][Full Text] [Related]
14. Confirmation of Kapur-Toriello syndrome in an Italian patient.
Zelante L; Candela MA; Savoia A; Gasparini P
Clin Dysmorphol; 1999 Apr; 8(2):151-3. PubMed ID: 10319207
[TBL] [Abstract][Full Text] [Related]
15. Two male siblings with cavum septum pellucidum, cavum vergae, macrocephaly, seizures and mental retardation. A new hereditary syndrome?
Sánchez O; Nastasi J; Escalona J; Guerra D
Clin Dysmorphol; 1997 Apr; 6(2):129-32. PubMed ID: 9134292
[TBL] [Abstract][Full Text] [Related]
16. Direct transmission of the 18q- syndrome from mother to daughter.
Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W
Genet Couns; 2006; 17(2):185-9. PubMed ID: 16970036
[TBL] [Abstract][Full Text] [Related]
17. Congenital contractures, short stature, abnormal face, microcephaly, scoliosis, hip dislocation, and severe psychomotor retardation in two unrelated girls. a new MCA/MR syndrome?
Mégarbané A; Ghanem I; Romana S; Gosset P; Caillaud C
Genet Couns; 2002; 13(2):123-31. PubMed ID: 12150211
[TBL] [Abstract][Full Text] [Related]
18. Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?
Moog U; Schoonbrood-Lenssen AM; Schrander-Stumpel CT; Fryns JP
Genet Couns; 1998; 9(3):211-3. PubMed ID: 9777344
[TBL] [Abstract][Full Text] [Related]
19. "New" ectodermal dysplasia with mental retardation and syndactyly.
Ilyina HG; Amoashy DS; Grygory HA
Am J Med Genet; 1995 Sep; 58(4):345-7. PubMed ID: 8533843
[TBL] [Abstract][Full Text] [Related]
20. Costello syndrome: report of a new case with choanal atresia and fatal outcome.
Boente MC; Carrero-Valenzuela RD; Frontini MV; Asial RA
Eur J Dermatol; 2001; 11(5):453-7. PubMed ID: 11525956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
