ID

45312

Beskrivning

Principal Investigator: Terri H. Beaty, PhD, Johns Hopkins University School of Public Health, Baltimore, MD, USA MeSH: Cleft Lip,Cleft Palate,Congenital Abnormalities,Stomatognathic System Abnormalities https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000459 Building upon our previous linkage and association studies, we will use whole exome sequencing studies of second and third degree affected relatives drawn from multiplex families. Our specific aims are: 1) To conduct whole exome sequencing on affected members (2° and 3° relatives) drawn from multiplex cleft families from a consortium to identify novel genes causing non-syndromic oral clefts; 2) To confirm and test the role of rare variants in these novel genes through confirmatory Sanger sequencing, plus linkage information using additional members available in these multiplex families. This whole exome sequencing approach will combine evidence from linkage studies and large scale sequencing to identify novel genes causing oral clefts in multiplex cleft families.

Länk

dbGaP study = phs000459

Nyckelord

  1. 2022-10-23 2022-10-23 - Adrian Schulz
Rättsinnehavare

Terri H. Beaty, PhD, Johns Hopkins University School of Public Health, Baltimore, MD, USA

Uppladdad den

23 oktober 2022

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

dbGaP phs000459 CIDR Whole Exome sequencing of multiplex cleft families

Eligibility Criteria

Inclusion and exclusion criteria
Beskrivning

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
All affected individuals were identified as having an isolated, non-syndromic oral cleft in the initial recruitment visit, although mis-classification is always possible. All families were reviewed by experienced geneticist(s) and there was no evidence of recognized Mendelian forms of oral clefts (e.g. Vander Woude syndrome), but even this level of phenotypic review can miss some forms of recognized Mendelian syndromes.
Beskrivning

Elig.phs000459.v1.p1.1

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3846158

Similar models

Eligibility Criteria

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000459.v1.p1.1
Item
All affected individuals were identified as having an isolated, non-syndromic oral cleft in the initial recruitment visit, although mis-classification is always possible. All families were reviewed by experienced geneticist(s) and there was no evidence of recognized Mendelian forms of oral clefts (e.g. Vander Woude syndrome), but even this level of phenotypic review can miss some forms of recognized Mendelian syndromes.
boolean
C3846158 (UMLS CUI [1,1])

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial