158 related articles for article (PubMed ID: 11477608)
1. Severe mental retardation, short stature, facial anomalies, joint laxity, and dislocations in two sisters: previously undescribed MCA/MR syndrome.
Mégarbané A; Cormier-Daire V
Am J Med Genet; 2001 Aug; 102(2):153-6. PubMed ID: 11477608
[TBL] [Abstract][Full Text] [Related]
2. Short stature, abnormal face, joint laxity, dislocation, hernias, delayed bone age, and severe psychomotor retardation in two brothers: previously undescribed MCA/MR syndrome.
Mégarbané A; Ruchoux MM; Loeys B; Ayoub N; Nuytinck L
Am J Med Genet; 2001 Dec; 104(3):221-4. PubMed ID: 11754048
[TBL] [Abstract][Full Text] [Related]
3. Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: a new autosomal recessive MCA/MR syndrome?
Kondoh T; Yamamoto T; Kono Y; Matsumoto T; Sugawara H; Matsumoto N; Moriuchi H
Am J Med Genet; 2001 Jul; 102(1):63-7. PubMed ID: 11471174
[TBL] [Abstract][Full Text] [Related]
4. Absence of thumbs, A/hypoplasia of radius, hypoplasia of ulnae, retarded bone age, short stature, microcephaly, hypoplastic genitalia, and mental retardation.
Wieczorek D; Köster B; Gillessen-Kaesbach G
Am J Med Genet; 2002 Mar; 108(3):209-13. PubMed ID: 11891687
[TBL] [Abstract][Full Text] [Related]
5. A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features.
Vinkler C; Leshinsky-Silver E; Michelson M; Haas D; Lerman-Sagie T; Lev D
Eur J Med Genet; 2014; 57(6):288-92. PubMed ID: 24709618
[TBL] [Abstract][Full Text] [Related]
6. Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome?
Zerres K; Rietschel M; Rietschel E; Majewski F; Meinecke P
J Med Genet; 1992 Apr; 29(4):269-71. PubMed ID: 1316441
[TBL] [Abstract][Full Text] [Related]
7. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
Meinecke P
Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
[TBL] [Abstract][Full Text] [Related]
8. New syndrome of mental retardation, Robin sequence, and brachydactyly.
Gurrieri F; Steindl K; Giglio S; Neri G
Am J Med Genet; 2001 Apr; 100(1):49-51. PubMed ID: 11337748
[TBL] [Abstract][Full Text] [Related]
9. X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.
Carpenter NJ; Qu Y; Curtis M; Patil SR
Am J Med Genet; 1999 Jul; 85(3):230-5. PubMed ID: 10398234
[TBL] [Abstract][Full Text] [Related]
10. Possible case of Pitt-Hopkins syndrome in sibs.
Orrico A; Galli L; Zappella M; Lam CW; Bonifacio S; Torricelli F; Hayek G
Am J Med Genet; 2001 Oct; 103(2):157-9. PubMed ID: 11568923
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mental retardation with pterygia, shortness and distinct facial appearance. Confirmation of a new MCA/MR syndrome.
Schrander-Stumpel C; Haspeslagh M; Fryns JP
Clin Genet; 1988 Oct; 34(4):279-81. PubMed ID: 3233782
[No Abstract] [Full Text] [Related]
13. Short stature, moderate mental retardation, hyperactivity, facial dysmorphism, skeletal abnormalities, and exaggerated ketosis: a new syndrome.
Boneh A; Glick B; Gutman A; Mogle P
Clin Genet; 1996 Nov; 50(5):403-6. PubMed ID: 9007332
[TBL] [Abstract][Full Text] [Related]
14. Post-natal short stature, short limbs, brachydactyly, facial abnormalities, and delayed bone age: a new syndrome?
Mégarbané A; Rassi S; Estephan F; Kouba-Hreich E
Am J Med Genet A; 2004 Feb; 125A(1):57-60. PubMed ID: 14755467
[TBL] [Abstract][Full Text] [Related]
15. Mental retardation with pterygia, shortness and distinct facial appearance. A new MCA/MR syndrome.
Haspeslagh M; Fryns JP; de Mûelenaere A; Schautteet L; van Eeckhoutte I; van den Berghe H
Clin Genet; 1985 Dec; 28(6):550-5. PubMed ID: 4075567
[TBL] [Abstract][Full Text] [Related]
16. Unusual type of brachydactyly associated with short stature and facial anomalies. A new syndrome?
Richieri-Costa A; Colletto GM; Otto PA
Am J Med Genet; 1985 Aug; 21(4):637-42. PubMed ID: 4025394
[TBL] [Abstract][Full Text] [Related]
17. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients.
Guion-Almeida ML; Zechi-Ceide RM; Richieri-Costa A
Am J Med Genet; 1999 Nov; 87(1):72-7. PubMed ID: 10528252
[TBL] [Abstract][Full Text] [Related]
18. Facial erythema associated with short stature, absent distal phalanx, dental and nail anomalies: case report and neuropsychological profile.
Lanzi G; Termine C; Capsoni C; Zoppello M; Sacchi SA; Danesino C
Clin Dysmorphol; 2005 Apr; 14(2):105-107. PubMed ID: 15770135
[TBL] [Abstract][Full Text] [Related]
19. Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome?
Fryns JP; Smeets E; Thiry P; Geutjens J; Vinken L; Van den Berghe H
Am J Med Genet; 1994 Jan; 49(1):91-3. PubMed ID: 8172258
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
