Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2)
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2)
Authors
Keywords
-
Journal
JOURNAL OF HUMAN GENETICS
Volume 59, Issue 12, Pages 667-674
Publisher
Springer Nature
Online
2014-10-16
DOI
10.1038/jhg.2014.92
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality
- (2011) A. Nicoulaz et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints
- (2010) Marzena Gajecka et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A study of meiotic segregation of chromosomes in spermatozoa of translocation carriers using fluorescentin situhybridisation
- (2010) A. Perrin et al. ANDROLOGIA
- Experiences with risk estimates for carriers of chromosomal reciprocal translocations
- (2010) Alina T. Midro et al. CLINICAL GENETICS
- Monosomy 10q26-qter and trisomy 11q13-qter as a result ofde novo unbalanced translocation
- (2010) F. Tinsa et al. JOURNAL OF APPLIED GENETICS
- Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements
- (2009) Carla S. D’Angelo et al. HUMAN GENETICS
- Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees
- (2008) Hartmut Engels et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation
- (2008) Emily Chen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36
- (2008) Shoji Saito et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Prenatal diagnosis of monosomy 1p36: A focus on brain abnormalities and a review of the literature
- (2008) Philippe M. Campeau et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2
- (2008) William B. Dobyns et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- DNA fragmentation and meiotic segregation in sperm of carriers of a chromosomal structural abnormality
- (2008) Aurore Perrin et al. FERTILITY AND STERILITY
- Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)
- (2008) M. Gajecka et al. GENOME RESEARCH
- Standardized Human Pedigree Nomenclature: Update and Assessment of the Recommendations of the National Society of Genetic Counselors
- (2008) Robin L. Bennett et al. Journal of Genetic Counseling
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More