154 related articles for article (PubMed ID: 7645600)
1. Mixed sclerosing bone dysplasia, small stature, seizure disorder, and mental retardation: a syndrome?
Jurenka SB; Van Allen MI
Am J Med Genet; 1995 May; 57(1):6-9. PubMed ID: 7645600
[TBL] [Abstract][Full Text] [Related]
2. Mosaic trisomy 15 in a short girl with hemihypotrophy and mental retardation.
Knauer-Fischer SA; Richter-Unruh A; Albrecht B; Gillessen-Kaesbach G; Hauffa BP
Clin Dysmorphol; 2004 Jul; 13(3):183-186. PubMed ID: 15194957
[TBL] [Abstract][Full Text] [Related]
3. Trisomy 18 mosaicism in a mildly retarded boy with postnatal overgrowth.
Plessis G; Le Treust M; Lemaire F; Maugard T; Cau D
Ann Genet; 1997; 40(4):235-7. PubMed ID: 9526621
[TBL] [Abstract][Full Text] [Related]
4. The chromosome 2 distal short arm trisomy syndrome.
Cassidy SB; Heller RM; Chazen EM; Engel E
J Pediatr; 1977 Dec; 91(6):934-8. PubMed ID: 925823
[TBL] [Abstract][Full Text] [Related]
5. Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation.
Mikelsaar RV; Varb K; Süvari A; Schinzel A
J Med Genet; 2001 Jan; 38(1):E2. PubMed ID: 11134241
[No Abstract] [Full Text] [Related]
6. A girl with 15q overgrowth syndrome and dup(15)(q24q26.3) that included telomeric sequences.
Gutiérrez-Franco Mde L; Madariaga-Campos Mde L; Vásquez-Velásquez AI; Matute E; Guevara-Yáñez R; Rivera H
Korean J Lab Med; 2010 Jun; 30(3):318-24. PubMed ID: 20603595
[TBL] [Abstract][Full Text] [Related]
7. [Genetic and prenatal diagnosis of a pregnant women with mental retardation].
Zhang L; Ren M; Song G; Liu X; Zhang J; Wang J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):674-7. PubMed ID: 27577220
[TBL] [Abstract][Full Text] [Related]
8. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardation.
Stoll C; Chognot D; Halb A; Luckel JC
J Med Genet; 1993 May; 30(5):433-5. PubMed ID: 8320712
[TBL] [Abstract][Full Text] [Related]
10. Trisomy 4q syndrome: presentation of a new case and review of the literature.
Lundin C; Zech L; Sjörs K; Wadelius C; Annerén G
Ann Genet; 2002; 45(2):53-7. PubMed ID: 12119211
[TBL] [Abstract][Full Text] [Related]
11. Trisomy-8 mosaicism: report of a case.
Silengo MC; Davi G; Crua G; Franceschini P
Hum Genet; 1978 Jun; 42(3):323-6. PubMed ID: 669713
[TBL] [Abstract][Full Text] [Related]
12. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability.
Chen CP; Lin SP; Chern SR; Tsai FJ; Lee MS; Chen YJ; Wang W
Genet Couns; 2011; 22(4):425-30. PubMed ID: 22303804
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome.
Nevin NC; Thomas PS; Hutchinson J
Am J Med Genet; 1986 May; 24(1):33-9. PubMed ID: 3706411
[TBL] [Abstract][Full Text] [Related]
15. A rare cause of short stature: Leri Weill dyschondrosteosis.
Cakir M; Kalyoncu M; Odemiş E; Okten A
Genet Couns; 2003; 14(2):215-20. PubMed ID: 12872816
[TBL] [Abstract][Full Text] [Related]
16. Mixed-sclerosing-bone-dystrophy: report of a case and review of the literature.
Whyte MP; Murphy WA; Fallon MD; Hahn TJ
Skeletal Radiol; 1981; 6(2):95-102. PubMed ID: 7256311
[TBL] [Abstract][Full Text] [Related]
17. 1q44-qter trisomy: clinical report and review of the literature.
Lenzini E; Ballarati L; Drigo P; Carrozzi M; Gambel-Benussi D; Giardino D; Petix V; Rizzotto MR; Pecile V
Genet Test Mol Biomarkers; 2009 Feb; 13(1):79-86. PubMed ID: 19309278
[TBL] [Abstract][Full Text] [Related]
18. Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.
Sogaard M; Tümer Z; Hjalgrim H; Hahnemann J; Friis B; Ledaal P; Pedersen VF; Baekgaard P; Tommerup N; Cingöz S; Duno M; Brondum-Nielsen K
BMC Med Genet; 2005 May; 6():21. PubMed ID: 15904506
[TBL] [Abstract][Full Text] [Related]
19. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
[TBL] [Abstract][Full Text] [Related]
20. Mental retardation, short stature and brittle hair (BIDS syndrome; hair brain syndrome).
Hora RK; Murthy VS
Indian J Pediatr; 1996; 63(1):117-20. PubMed ID: 10829976
[No Abstract] [Full Text] [Related]
[Next] [New Search]
