134 related articles for article (PubMed ID: 6182156)
1. A recurrent pattern syndrome of craniosynostosis associated with arachnodactyly and abdominal hernias.
Shprintzen RJ; Goldberg RB
J Craniofac Genet Dev Biol; 1982; 2(1):65-74. PubMed ID: 6182156
[TBL] [Abstract][Full Text] [Related]
2. Marfanoid features and craniosynostosis: report of one case and review.
Lacombe D; Battin J
Clin Dysmorphol; 1993 Jul; 2(3):220-4. PubMed ID: 8287183
[TBL] [Abstract][Full Text] [Related]
3. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
4. New Marfanoid syndrome with craniosynostosis.
Furlong J; Kurczynski TW; Hennessy JR
Am J Med Genet; 1987 Mar; 26(3):599-604. PubMed ID: 3565476
[TBL] [Abstract][Full Text] [Related]
5. Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable types.
Verloes A; Journel H; Elmer C; Misson JP; Le Merrer M; Kaplan J; Van Maldergem L; Deconinck H; Meire F
Am J Med Genet; 1993 Apr; 46(2):132-7. PubMed ID: 8484397
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Two unrelated children with developmental delay, short stature and anterior chamber cleavage disorder, cerebellar hypoplasia, endocrine disturbances and tracheostenosis: a new entity?
Jung C; Wolff G; Back E; Stahl M
Clin Dysmorphol; 1995 Jan; 4(1):44-51. PubMed ID: 7537583
[TBL] [Abstract][Full Text] [Related]
8. Possible third case of Lin-Gettig syndrome.
Hedera P; Innis JW
Am J Med Genet; 2002 Jul; 110(4):380-3. PubMed ID: 12116213
[TBL] [Abstract][Full Text] [Related]
9. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
Jonas RE; Kimonis VE; Morales A
Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
[TBL] [Abstract][Full Text] [Related]
10. Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation.
Kosztolányi G; Weisenbach J; Méhes K
Am J Med Genet; 1995 Sep; 58(3):213-6. PubMed ID: 8533819
[TBL] [Abstract][Full Text] [Related]
11. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
Schinzel A; Schmid W
Am J Med Genet; 1980; 6(3):241-9. PubMed ID: 7424976
[TBL] [Abstract][Full Text] [Related]
12. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
Fryburg JS; Golden WL
Am J Med Genet; 1993 Mar; 45(5):638-41. PubMed ID: 7681252
[TBL] [Abstract][Full Text] [Related]
13. Pseudoaminopterin syndrome.
Verloes A; Bricteux G; Koulischer L
Am J Med Genet; 1993 Jun; 46(4):394-7. PubMed ID: 8357010
[TBL] [Abstract][Full Text] [Related]
14. Thoraco-abdominal aortic aneurysm rupture in a patient with Shprintzen-Goldberg syndrome.
Kimura N; Inaba Y; Kameyama K; Shimizu H
Interact Cardiovasc Thorac Surg; 2018 Jun; 26(6):1039-1040. PubMed ID: 29346558
[TBL] [Abstract][Full Text] [Related]
15. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
Steinbach P; Wolf M; Schmidt H
Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
[TBL] [Abstract][Full Text] [Related]
16. Developmental delay in fetal aminopterin/methotrexate syndrome.
Del Campo M; Kosaki K; Bennett FC; Jones KL
Teratology; 1999 Jul; 60(1):10-2. PubMed ID: 10413333
[TBL] [Abstract][Full Text] [Related]
17. [Joubert's syndrome: report of 12 cases].
Barreirinho MS; Teixeira J; Moreira NC; Bastos S; Gonçalvez S; Barbot MC
Rev Neurol; 2001 May 1-15; 32(9):812-7. PubMed ID: 11424029
[TBL] [Abstract][Full Text] [Related]
18. Craniosynostosis and marfanoid habitus without mental retardation: report of a third case.
Mégarbané A; Hokayem N
Am J Med Genet; 1998 May; 77(2):170-1. PubMed ID: 9605294
[No Abstract] [Full Text] [Related]
19. Third case of Pfeiffer-type cardiocranial syndrome.
Stratton RF; Parsons DS
Am J Med Genet; 1989 Dec; 34(4):587-8. PubMed ID: 2624274
[TBL] [Abstract][Full Text] [Related]
20. [Arachnodactyly associated with mental disorders].
Markupová H; Krízek J; Volfová J
Cesk Psychiatr; 1966 Oct; 62(5):329-30. PubMed ID: 5977496
[No Abstract] [Full Text] [Related]
[Next] [New Search]
