134 related articles for article (PubMed ID: 12238251)
1. [Mosaic phenotypes].
Seemanová E
Cas Lek Cesk; 2002 Jul; 141(14):439-44. PubMed ID: 12238251
[TBL] [Abstract][Full Text] [Related]
2. [Microdeletion syndromes].
Seemanová E
Cas Lek Cesk; 2002 Jun; 141(12):363-70. PubMed ID: 12238021
[TBL] [Abstract][Full Text] [Related]
3. Mosaics and haemophilia.
Kasper CK; Buzin CH
Haemophilia; 2009 Nov; 15(6):1181-6. PubMed ID: 19473426
[TBL] [Abstract][Full Text] [Related]
4. [Current interpretation of mosaicism].
Méhes K; Kosztolányi G
Orv Hetil; 1990 Aug; 131(33):1815-9. PubMed ID: 2204862
[TBL] [Abstract][Full Text] [Related]
5. Mosaicism in human skin. Understanding the patterns and mechanisms.
Happle R
Arch Dermatol; 1993 Nov; 129(11):1460-70. PubMed ID: 8239703
[TBL] [Abstract][Full Text] [Related]
6. Unilateral microtia in an infant with trisomy 18 mosaicism.
Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
[TBL] [Abstract][Full Text] [Related]
7. Pigmentary mosaicism of the hyperpigmented type in two half-brothers.
Horn D; Happle R; Neitzel H; Kunze J
Am J Med Genet; 2002 Sep; 112(1):65-9. PubMed ID: 12239723
[TBL] [Abstract][Full Text] [Related]
8. Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case.
Martínez A; Ramos S; González-del Angel A; Alcántara MA; Molina B; Carnevale A
Rev Invest Clin; 2007; 59(6):444-8. PubMed ID: 18402336
[TBL] [Abstract][Full Text] [Related]
9. [Y chromosome structural abnormalities and Turner's syndrome].
Ravel C; Siffroi JP
Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
[TBL] [Abstract][Full Text] [Related]
10. Somatic APC mosaicism: an underestimated cause of polyposis coli.
Hes FJ; Nielsen M; Bik EC; Konvalinka D; Wijnen JT; Bakker E; Vasen HF; Breuning MH; Tops CM
Gut; 2008 Jan; 57(1):71-6. PubMed ID: 17604324
[TBL] [Abstract][Full Text] [Related]
11. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
[TBL] [Abstract][Full Text] [Related]
12. APC somatic mosaicism in a patient with Gardner syndrome carrying the E1573X mutation: report of a case.
Filipe B; Albuquerque C; Bik E; Lage P; Rodrigues P; Vossen R; Tops C; Nobre Leitão C
Dis Colon Rectum; 2009 Aug; 52(8):1516-20; discussion 1520-1. PubMed ID: 19617769
[TBL] [Abstract][Full Text] [Related]
13. Trisomy 14 Mosaicism: a case without evidence of neurodevelopmental delay and a review of the literature.
Merritt TA; Natarajan G
Am J Perinatol; 2007 Oct; 24(9):563-6. PubMed ID: 17893842
[TBL] [Abstract][Full Text] [Related]
14. Accuracy of perinatal diagnosis of 45,X/46,XY mosaicism and electronic consultation of affected parents.
Kibar Y; Frimberger D; Kropp BP; Reiner W
J Pediatr Urol; 2009 Aug; 5(4):274-8. PubMed ID: 19329364
[TBL] [Abstract][Full Text] [Related]
15. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
Kulharya AS; Lovell CM; Flannery DB
Am J Med Genet; 2002 Dec; 113(4):367-70. PubMed ID: 12457409
[TBL] [Abstract][Full Text] [Related]
16. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
[TBL] [Abstract][Full Text] [Related]
17. Phenotypic variability in isodicentric Y patients: study of nine cases.
DesGroseilliers M; Beaulieu Bergeron M; Brochu P; Lemyre E; Lemieux N
Clin Genet; 2006 Aug; 70(2):145-50. PubMed ID: 16879197
[TBL] [Abstract][Full Text] [Related]
18. A cryptic full mutation in a male with a classical fragile X phenotype.
MacKenzie JJ; Sumargo I; Taylor SA
Clin Genet; 2006 Jul; 70(1):39-42. PubMed ID: 16813602
[TBL] [Abstract][Full Text] [Related]
19. Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.
Grati FR; Grimi B; Frascoli G; Di Meco AM; Liuti R; Milani S; Trotta A; Dulcetti F; Grosso E; Miozzo M; Maggi F; Simoni G
Eur J Hum Genet; 2006 Mar; 14(3):282-8. PubMed ID: 16418738
[TBL] [Abstract][Full Text] [Related]
20. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
Wimplinger I; Rauch A; Orth U; Schwarzer U; Trautmann U; Kutsche K
Eur J Med Genet; 2007; 50(6):421-31. PubMed ID: 17845869
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
