نتایج جستجو برای: incomplete penetrance

تعداد نتایج: 61081  

2011
Ruihua Dang Daisuke Torigoe Nobuya Sasaki Takashi Agui

Hirschsprung disease (HSCR) exhibits complex genetics with incomplete penetrance and variable severity thought to result as a consequence of multiple gene interactions that modulate the ability of enteric neural crest cells to populate the developing gut. As reported previously, when the same null mutation of the Ednrb gene, Ednrb(sl), was introgressed into the F344 strain, almost 60% of F344-E...

Journal: :Clinical genetics 2016
M Lefebvre D Sanlaville N Marle C Thauvin-Robinet E Gautier S E Chehadeh A-L Mosca-Boidron J Thevenon P Edery M-P Alex-Cordier M Till S Lyonnet V Cormier-Daire J Amiel A Philippe S Romana V Malan A Afenjar S Marlin S Chantot-Bastaraud P Bitoun B Heron E Piparas F Morice-Picard S Moutton N Chassaing A Vigouroux-Castera J Lespinasse S Manouvrier-Hanu O Boute-Benejean C Vincent-Delorme F Petit N L Meur M Marti-Dramard A-M Guerrot A Goldenberg S Redon C Ferrec S Odent C L Caignec S Mercier B Gilbert-Dussardier A Toutain S Arpin S Blesson I Mortemousque E Schaefer D Martin N Philip S Sigaudy T Busa C Missirian F Giuliano H K Benailly P K V Kien B Leheup C Benneteau L Lambert R Caumes P Kuentz I François D Heron B Keren E Cretin P Callier S Julia L Faivre

Microarray-based comparative genomic hybridization (aCGH) is commonly used in diagnosing patients with intellectual disability (ID) with or without congenital malformation. Because aCGH interrogates with the whole genome, there is a risk of being confronted with incidental findings (IF). In order to anticipate the ethical issues of IF with the generalization of new genome-wide analysis technolo...

Journal: :Development 2007
John W Chandler Melanie Cole Annegret Flier Britta Grewe Wolfgang Werr

DORNROSCHEN (DRN) (also known as ENHANCER OF SHOOT REGENERATION1; ESR1) and DRN-LIKE (DRNL; also known as ESR2) are two linked paralogues encoding AP2 domain-containing proteins. drn mutants show embryo cell patterning defects and, similarly to drnl mutants, disrupt cotyledon development at incomplete penetrance. drn drnl double mutants with weak or strong drnl alleles show more highly penetran...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
F R Goodman S Mundlos Y Muragaki D Donnai M L Giovannucci-Uzielli E Lapi F Majewski J McGaughran C McKeown W Reardon J Upton R M Winter B R Olsen P J Scambler

Synpolydactyly (SPD) is a dominantly inherited congenital limb malformation. Typical cases have 3/4 finger and 4/5 toe syndactyly, with a duplicated digit in the syndactylous web, but incomplete penetrance and variable expressivity are common. The condition has recently been shown to be caused by expansions of an imperfect trinucleotide repeat sequence encoding a 15-residue polyalanine tract in...

2013
Cheri Deal

DICER1 is an RNase endonuclease important for production of microRNAs, which regulate multiple proteincoding genes involved in growth and development. It has been linked to several tumors including pleuropulmonary blastoma (PPB), cystic nephroma, ovarian Sertoli-Leydig cell tumors and thyroid neoplasia. Most of the manifestations of DICER1 mutations occur in young children, adolescents and youn...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1994
M Muenke F Gurrieri C Bay D H Yi A L Collins V P Johnson R C Hennekam G B Schaefer L Weik M S Lubinsky

Holoprosencephaly (HPE) is a common malformation of the developing forebrain and midface characterized by incomplete penetrance and variable expressivity. Familial HPE has been reported in many families with autosomal dominant inheritance in some and apparent autosomal recessive inheritance in others. We have examined 125 individuals from nine families with autosomal dominant HPE. Expression in...

Journal: :Progress in neurobiology 2012
Hannah M Grayton Cathy Fernandes Dan Rujescu David A Collier

Common neurodevelopmental disorders (including autism, speech and language delay, schizophrenia, epilepsy and intellectual disability) have complex aetiology, which is predominantly genomic, but also environmental in origin. They share a paradox, in that high heritability is matched by lowered fecundity, placing them under negative genetic selection. This implicates variants of recent origin, s...

2014
Victor A. David Marilyn Menotti-Raymond Andrea Coots Wallace Melody Roelke James Kehler Robert Leighty Eduardo Eizirik Steven S. Hannah George Nelson Alejandro A. Schäffer Catherine J. Connelly Stephen J. O’Brien David K. Ryugo

The Dominant White locus (W) in the domestic cat demonstrates pleiotropic effects exhibiting complete penetrance for absence of coat pigmentation and incomplete penetrance for deafness and iris hypopigmentation. We performed linkage analysis using a pedigree segregating White to identify KIT (Chr. B1) as the feline W locus. Segregation and sequence analysis of the KIT gene in two pedigrees (P1 ...

2018
Adel Shalata Mohammad Mahroom Dianna M Milewicz Gong Limin Fadi Kassum Khader Badarna Nader Tarabeih Nimmer Assy Rona Fell Hector Cohen Munir Nashashibi Alejandro Livoff Muhammad Azab George Habib Dan Geiger Omer Weissbrod William Nseir

BACKGROUND Thoracic and abdominal aortic aneurysms and dissection often develop in hypertensive elderly patients. At higher risk are smokers and those who have a family history of aortic aneurysms. In most affected families, the aortic aneurysms and dissection is inherited in an autosomal dominant manner with decreased penetrance and variable expressivity. Mutations at two chromosomal loci, TAA...

Journal: :Human molecular genetics 1998
R E Ferrell K L Levinson J H Esman M A Kimak E C Lawrence M M Barmada D N Finegold

Hereditary or primary lymphedema is a developmental disorder of the lymphatic system which leads to a disabling and disfiguring swelling of the extremities. Hereditary lymphedema generally shows an autosomal dominant pattern of inheritance with reduced penetrance, variable expression and variable age at onset. Three multigeneration families demonstrating the phenotype of hereditary lymphedema s...

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