(Q36830976)

English

Urinary tract abnormalities (UTA) and associated malformations: data of the Emilia-Romagna Registry. IMER Group. Emilia-Romagna Registry on Congenital Malformations

scientific article published on October 1996

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Urinary tract abnormalities (UTA) and associated malformations: data of the Emilia-Romagna Registry. IMER Group. Emilia-Romagna Registry on Congenital Malformations (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

congenital disorder

0 references

author name string

Cocchi G

1

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Magnani C

2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Morini MS

3

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Garani GP

4

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Milan M

5

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Calzolari E

6

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

publication date

1 October 1996

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

European Journal of Epidemiology

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

493-497

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Echocardiographic Findings in Autosomal Dominant Polycystic Kidney Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial caudal regression anomalad and maternal diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malformations of kidney and urinary tract in common chromosomal aberrations. I. Clinical studies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The branchio-oto-renal (BOR) syndrome: report of bilateral renal agenesis in three sibs

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Embryologic pathogenesis of renal agenesis associated with cervical vertebral anomalies (Klippel-Feil phenotype)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urological diagnosis in utero

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vascular steal: the pathogenetic mechanism producing sirenomelia and associated defects of the viscera and soft tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The changing sonographic appearance of fetal kidneys during pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant polycystic kidney disease: early diagnosis and data for genetic counselling

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postnatal Ultrasound Screening of Urinary Malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Value of antenatal diagnosis of abnormalities of the urinary tract

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital appearance of adult-type (autosomal dominant) polycystic kidney disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital urinary tract malformations: epidemiologic and genetic aspects*

1 reference

https://pubmed.ncbi.nlm.nih.gov/8905311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00144002

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

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