(Q35015902)

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Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34

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5 August 2017

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Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34 (English)

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5 August 2017

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Stilianos Antonarakis

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Stylianos E Antonarakis

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Uppala Radhakrishna

1

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5 August 2017

Uppala Ratnamala

2

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5 August 2017

Mathew Gaines

3

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5 August 2017

Soraya Beiraghi

4

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5 August 2017

David Hutchings

5

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5 August 2017

Jeffrey Golla

6

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5 August 2017

Syed A Husain

7

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5 August 2017

Prakash S Gambhir

8

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5 August 2017

Jayesh J Sheth

9

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5 August 2017

Frenny J Sheth

10

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5 August 2017

Ghati K Chetan

11

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5 August 2017

Mohammed Naveed

12

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5 August 2017

Jitendra V Solanki

13

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5 August 2017

Uday C Patel

14

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5 August 2017

Dilipkumar C Master

15

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5 August 2017

Rafiq Memon

16

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5 August 2017

Gregory S Antonarakis

17

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5 August 2017

Swapan K Nath

19

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publication date

21 July 2006

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5 August 2017

American Journal of Human Genetics

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5 August 2017

79

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5 August 2017

3

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5 August 2017

580-585

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Europe PubMed Central

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5 August 2017

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Variation in IRF6 contributes to nonsyndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Gene/environment causes of cleft lip and/or palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Phylloid pattern of pigmentary disturbance in a case of complex mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

A locus for isolated cleft palate, located on human chromosome 2q32

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Partial trisomy 13q identified by sequential fluorescence in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

10p duplication characterized by fluorescence in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Familial t(4;13) with abnormal offspring in three generations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Autosomal trisomy 18 and 13 syndromes in Ibadan, Nigeria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Trisomy for the proximal segment of the long arm of chromosome 13: a new entity?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Trisomy for the distal segment of chromosome 13: a new syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Effects of misspecifying genetic parameters in lod score analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

The gene responsible for X-linked cleft palate (CPX) in a British Columbia native kindred is localized between PGK1 and DXYS1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

8 July 2018

Nonsyndromic cleft lip and palate: four chromosomal regions of interest

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

Association of chromosomal regions 3p21.2, 10p13, and 16p13.3 with nonsyndromic cleft lip and palate.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

The impact of SNP density on fine-scale patterns of linkage disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

Caution on pedigree haplotype inference with software that assumes linkage equilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

[Association of non-syndromic cleft lip and cleft palate with microsatellite markers located in 6p]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

A locus in 2p13-p14 (OFC2), in addition to that mapped in 6p23, is involved in nonsyndromic familial orofacial cleft malformation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

25 October 2018

Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

9 December 2018

A first-generation linkage disequilibrium map of human chromosome 22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559556

9 December 2018

How to model a complex trait. 2. Analysis with two disease loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible localization of a major gene for cleft lip and palate to 4q

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal defects and associated malformations in fetal cleft lip with or without cleft palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial distal trisomy 13q resulting from familial reciprocal 5/13 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 13q21?qter de novo due to a recombinant chromosome rec(13)dup q

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of an X-chromosome cleft palate gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suggestive linkage between markers on chromosome 19q13.2 and nonsyndromic orofacial cleft malformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary dentition status and treatment needs of children with cleft lip and/or palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal cleft lip and palate: sonographic diagnosis, chromosomal abnormalities, associated anomalies and postnatal outcome in 70 fetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsyndromic cleft lip with or without cleft palate in China: assessment of candidate regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome‐wide scan for loci predisposing to non‐syndromic cleft lip with or without cleft palate in two large Syrian families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

1 reference

https://pubmed.ncbi.nlm.nih.gov/16909398

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

ResearchGate publication ID

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