290 related articles for article (PubMed ID: 437787)
1. Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.
Fryns JP; Van den Berghe H
Hum Genet; 1979 Mar; 47(2):213-6. PubMed ID: 437787
[TBL] [Abstract][Full Text] [Related]
2. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
Fryns JP; Casaer P; Van den Berghe H
Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
[TBL] [Abstract][Full Text] [Related]
3. Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)/46,XX.
Balci S; Tümer C; Karaca C; Bartsch O
Am J Med Genet A; 2011 May; 155A(5):1129-35. PubMed ID: 21484996
[TBL] [Abstract][Full Text] [Related]
4. 46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study.
Kashevarova AA; Nikitina TV; Mikhailik LI; Belyaeva EO; Vasilyev SA; Lopatkina ME; Fedotov DA; Fonova EA; Zarubin AA; Sivtsev AA; Skryabin NA; Nazarenko LP; Lebedev IN
Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33316910
[TBL] [Abstract][Full Text] [Related]
5. A cytogenetic survey of 200 unclassifiable mentally retarded children with congenital anomalies and 200 normal controls.
Tharapel AT; Summitt RL
Hum Genet; 1977 Jul; 37(3):329-38. PubMed ID: 885553
[TBL] [Abstract][Full Text] [Related]
6. Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, + i(8p)/46,XY.
Kristoffersson U; Lagergren J; Heim S; Mandahl N
Clin Genet; 1988 Sep; 34(3):201-3. PubMed ID: 3180507
[TBL] [Abstract][Full Text] [Related]
7. Transmission of ring 14 chromosome from mother to two sons.
Matalon R; Supple P; Wyandt H; Rosenthal IM
Am J Med Genet; 1990 Aug; 36(4):381-5. PubMed ID: 2202211
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.
Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):856-860. PubMed ID: 28040133
[TBL] [Abstract][Full Text] [Related]
9. Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.
Summitt RL; Tharapel AT; Wilroy RS
Eur J Pediatr; 1977 Jul; 125(3):169-74. PubMed ID: 885143
[TBL] [Abstract][Full Text] [Related]
10. 46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome.
Maaswinkel-Mooij PD; de Jong P; Beverstock GC
Clin Genet; 1993 Feb; 43(2):76-8. PubMed ID: 8448905
[TBL] [Abstract][Full Text] [Related]
11. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
Koç A; Kan D; Karaer K; Ergün MA; Karaoğuz MY; Gücüyener K; Hinreiner S; Liehr T; Perçin EF
Eur J Pediatr; 2008 Jun; 167(6):655-9. PubMed ID: 17668239
[TBL] [Abstract][Full Text] [Related]
12. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
Fryns JP; Kleczkowska A
Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841
[TBL] [Abstract][Full Text] [Related]
13. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
Jenderny J; Caliebe A; Beyer C; Grote W
J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656
[TBL] [Abstract][Full Text] [Related]
14. Emanuel syndrome due to unusual segregation of paternal origin.
Zaki MS; Mohamed AM; Kamel AK; El-Gerzawy AM; El-Ruby MO
Genet Couns; 2012; 23(2):319-28. PubMed ID: 22876593
[TBL] [Abstract][Full Text] [Related]
15. A profoundly mentally handicapped woman with a ring chromosome 22.
Veall RM; Rundle AT; Chitham RC; Saldana-Garcia P
J Ment Defic Res; 1975; 19(3-4):225-43. PubMed ID: 1214291
[TBL] [Abstract][Full Text] [Related]
16. Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.
Fryns JP; Kleczkowska A; Smeets E; Van Den Berghe H
Ann Genet; 1992; 35(2):121-3. PubMed ID: 1524410
[TBL] [Abstract][Full Text] [Related]
17. Analysis of banding patterns and mosaic configurations in a case of ring chromosome 15.
Schmid M; Henrichs I; Nestler H; Knörr-Gärtner H; Teller WM; Krone W
Hum Genet; 1978 Apr; 41(3):289-99. PubMed ID: 649157
[TBL] [Abstract][Full Text] [Related]
18. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.
Hobolth N; Jacobsen P; Mikkelsen M
J Med Genet; 1974 Sep; 11(3):299-303. PubMed ID: 4139263
[TBL] [Abstract][Full Text] [Related]
19. Ring chromosome 4.
McDermott A; Voyce MA; Romain D
J Med Genet; 1977 Jun; 14(3):228-32. PubMed ID: 881718
[TBL] [Abstract][Full Text] [Related]
20. Bisatellited dicentric chromosome: a report on a case with karyotype 47,XY, + psu dic(22)t(22;22)(22pter to cen to 22q11::22q11 to 22pter).
Weilong G; Aide Y; Hongbao F; Shumou L; Ju Y
Hum Genet; 1982; 61(4):325-8. PubMed ID: 7152517
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
