(Q34464512)

2 August 2017

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title

Normal and abnormal development of the urogenital tract (English)

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2 August 2017

Cuckow PM

1

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2 August 2017

Nyirady P

series ordinal

2

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2 August 2017

Winyard PJ

series ordinal

3

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2 August 2017

publication date

1 November 2001

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2 August 2017

number of pages

9

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based on heuristic

inferred from page(s)

published in

Prenatal Diagnosis

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2 August 2017

volume

21

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2 August 2017

issue

11

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2 August 2017

page(s)

908-916

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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

2 August 2017

cites work

1 reference

Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families

21 January 2018

1 reference

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci

21 January 2018

1 reference

SOX9 directly regulates the type-II collagen gene

21 January 2018

1 reference

Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta

21 January 2018

1 reference

Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease

21 January 2018

1 reference

Disorders of peroxisome biogenesis

21 January 2018

1 reference

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

21 January 2018

1 reference

KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development.

21 January 2018

1 reference

The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.

21 January 2018

1 reference

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

21 January 2018

1 reference

Identification of the gene for oral-facial-digital type I syndrome

21 January 2018

1 reference

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Programmed cell death in animal development

21 January 2018

1 reference

Genitourinary abnormalities associated with the Smith-Lemli-Opitz syndrome

21 January 2018

1 reference

Expression of hepatocyte growth factor/scatter factor and its receptor, MET, suggests roles in human embryonic organogenesis.

21 January 2018

1 reference

WT-1 is required for early kidney development

21 January 2018

1 reference

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

21 January 2018

1 reference

Duplex Kidneys: A Correlation of Renal Dysplasia with Position of the Ureteral Orifice

21 January 2018

1 reference

Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter

21 January 2018

1 reference

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

21 January 2018

1 reference

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

21 January 2018

1 reference

Multiple roles for the Wilms' tumour suppressor gene, WT1 in genitourinary development.

21 January 2018

1 reference

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

21 January 2018

1 reference

Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair

21 January 2018

1 reference

The PAX2 tanscription factor is expressed in cystic and hyperproliferative dysplastic epithelia in human kidney malformations

21 January 2018

1 reference

Deregulation of cell survival in cystic and dysplastic renal development.

21 January 2018

1 reference

Potential biological role of transforming growth factor-beta1 in human congenital kidney malformations

21 January 2018

1 reference

Dominantly inherited renal adysplasia

21 January 2018

1 reference

Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definition

21 January 2018

1 reference

Multicystic dysplastic kidney and Kallmann's syndrome: a new association?

21 January 2018

1 reference

Renal abnormalities on obstetric ultrasound as a presentation of DiGeorge syndrome

21 January 2018

1 reference

Unilateral renal aplasia in X-linked Kallmann's syndrome

21 January 2018

1 reference

Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men

21 January 2018

1 reference

Reduced Pax2 gene dosage increases apoptosis and slows the progression of renal cystic disease

21 January 2018

1 reference

The natural history of the multicystic dysplastic kidney in children

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PD.214

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2 August 2017

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