176 related articles for article (PubMed ID: 9007332)
1. 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]
2. Novel findings in a patient with Weaver or a Weaver-like syndrome.
Scarano G; Della Monica M; Lonardo F; Neri G
Am J Med Genet; 1996 May; 63(2):378-81. PubMed ID: 8725789
[TBL] [Abstract][Full Text] [Related]
3. Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred. A variant of K.B.G. syndrome or a new mental retardation syndrome.
Parloir C; Fryns JP; Deroover J; Lebas E; Goffaux P; van den Berghe H
Clin Genet; 1977 Nov; 12(5):263-6. PubMed ID: 589847
[TBL] [Abstract][Full Text] [Related]
4. Hunter-McAlpine syndrome: report of a third family.
Adès LC; Morris LL; Simpson DA; Haan EA
Clin Dysmorphol; 1993 Apr; 2(2):123-30. PubMed ID: 8281273
[TBL] [Abstract][Full Text] [Related]
5. Myhre syndrome: new reports, review, and differential diagnosis.
Burglen L; Héron D; Moerman A; Dieux-Coeslier A; Bourguignon JP; Bachy A; Carel JC; Cormier-Daire V; Manouvrier S; Verloes A
J Med Genet; 2003 Jul; 40(7):546-51. PubMed ID: 12843331
[No Abstract] [Full Text] [Related]
6. 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]
7. Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome.
García-Ortiz JE; Castañeda-Cisneros G; López-Cardona MG; Sánchez-Corona J; Patiño-García B; García-González CL; Nazará Z; Dávalos-Rodríguez N; Rodríguez LX; García-Cruz D
Am J Med Genet A; 2006 Jun; 140(11):1245-9. PubMed ID: 16688750
[No Abstract] [Full Text] [Related]
8. 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]
9. Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome?
Fryns JP; Haspeslagh M
Clin Genet; 1984 Jul; 26(1):69-72. PubMed ID: 6467660
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Split hand malformation, hypospadias, microphthalmia, distinctive face and short stature in two brothers suggest a new syndrome.
García-Ortiz JE; Banda-Espinoza F; Zenteno JC; Galván-Uriarte LM; Ruiz-Flores P; García-Cruz D
Am J Med Genet A; 2005 May; 135(1):21-7. PubMed ID: 15809993
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Marshall-Smith syndrome].
Saitoh S
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):211-2. PubMed ID: 11057200
[No Abstract] [Full Text] [Related]
16. Vohwinkel syndrome with mental retardation.
Mercy P; Singh A; Ghorpade AK; Das MN; Upadhyay A; Keswani N
Indian J Dermatol Venereol Leprol; 2013; 79(5):725. PubMed ID: 23974601
[No Abstract] [Full Text] [Related]
17. An unknown combination of infantile spasms, retinal lesions, facial dysmorphism and limb abnormalities.
Plomp AS; Reardon W; Benton S; Taylor D; Larcher VF; Sundrum R; Winter RM
Clin Dysmorphol; 2000 Jul; 9(3):189-92. PubMed ID: 10955479
[TBL] [Abstract][Full Text] [Related]
18. Filippi syndrome: a new case with skeletal abnormalities.
Héron D; Billette de Villemeur T; Munnich A; Lyonnet S
J Med Genet; 1995 Aug; 32(8):659-61. PubMed ID: 7473664
[TBL] [Abstract][Full Text] [Related]
19. [Ruvalcaba syndrome].
Ishii T
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):244-5. PubMed ID: 11057214
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]