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1. Full Text Advantages of Magnetic Resonance Imaging (MRI) of the Seminal Vesicles and Intra-abdominal Vas Deferens in Patients With Congenital Absence of the Vas Deferens
by Chiang, Han-Sun and Lin, Yi-Hsiang and Wu, Yi-No and Wu, Chien-Chih and Liu, Ming-Che and Lin, Chih-Ming
Urology (Ridgewood, N.J.), ISSN 0090-4295, 2013, Volume 82, Issue 2, pp. 345 - 351
Urology | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Nephrology. Urinary tract diseases | Biological and medical sciences | Medical sciences | Genetic Testing | Endosonography | Humans | Middle Aged | Vas Deferens - abnormalities | Male | Seminal Vesicles - abnormalities | Magnetic Resonance Imaging | Abnormalities, Multiple - diagnosis | Seminal Vesicles - diagnostic imaging | Vas Deferens - diagnostic imaging | Adult | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Abnormalities, Multiple - genetics | Medical colleges | Care and treatment | Genetic disorders | Magnetic resonance imaging | Index Medicus
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2. Full Text Beware the Looping Vas Deferens in Orchidopexy
by Cundy, Thomas P, MBBS PhD and Goh, Day Way, FRACS
Urology (Ridgewood, N.J.), ISSN 0090-4295, 2017, Volume 104, pp. 194 - 195
Urology | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Epididymis - surgery | Laparoscopy - methods | Testis - abnormalities | Urologic Surgical Procedures | Cryptorchidism - surgery | Humans | Vas Deferens - abnormalities | Child, Preschool | Male | Orchiopexy | Inguinal Canal - abnormalities | Index Medicus
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3. Full Text Genetics of the congenital absence of the vas deferens
by Bieth, Eric and Hamdi, Safouane M and Mieusset, Roger
Human genetics, ISSN 0340-6717, 02/2020, Volume 140, Issue 1, pp. 59 - 76
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Animals | Cystic Fibrosis - genetics | Humans | Vas Deferens - abnormalities | Azoospermia - genetics | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Male | Receptors, G-Protein-Coupled - genetics | Mutation - genetics | Male Urogenital Diseases - genetics | Cystic fibrosis | Genetic aspects | Genetic disorders | Genetic counseling | Infertility | Fetuses | Degeneration | Mutation | Diagnosis | Ultrasound | Vas deferens | Genetic screening | Organogenesis | Index Medicus | Review
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4. Full Text Ectopic Vas Deferens Inserting Into Distal Retroiliac Ureter in the Currarino Syndrome
by Alonso, Veronica and Perez, Sonia and Barrero, Rafael and Garcia-Merino, Francisco
Urology (Ridgewood, N.J.), ISSN 0090-4295, 2016, Volume 98, pp. 167 - 169
Urology | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Cystography | Ureter - abnormalities | Urogenital Abnormalities - diagnosis | Humans | Urologic Surgical Procedures, Male - methods | Vas Deferens - abnormalities | Abnormalities, Multiple | Cystoscopy | Male | Sacrum - abnormalities | Ureter - surgery | Rectum - abnormalities | Anal Canal - abnormalities | Digestive System Abnormalities - diagnosis | Vas Deferens - surgery | Urogenital Abnormalities - surgery | Vas Deferens - diagnostic imaging | Radioisotope Renography | Ureter - diagnostic imaging | Syringomyelia - diagnosis | Vasectomy - methods | Genetic disorders | Vasectomy | Index Medicus
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5. Full Text Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies
by Gajbhiye, Rahul and Kadam, Kaushiki and Khole, Aalok and Gaikwad, Avinash and Kadam, Seema and Shah, Rupin and Kumaraswamy, Rangaswamy and Khole, Vrinda
Indian journal of medical research (New Delhi, India : 1994), ISSN 0971-5916, 11/2016, Volume 143, Issue 5, pp. 616 - 623
Congenital absence of seminal vesicles | Unilateral renal agenesis | Ectopic kidney | Cystic fibrosis transmembrane conductance regulator gene | Congenital bilateral absence of vas deferens | Immunology | Life Sciences & Biomedicine | Medicine, General & Internal | General & Internal Medicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Vas Deferens - pathology | Kidney - pathology | Kidney Diseases - congenital | Kidney Diseases - pathology | Humans | Vas Deferens - abnormalities | Male | Infertility, Male - pathology | Congenital Abnormalities - pathology | Kidney Diseases - genetics | Congenital Abnormalities - genetics | Infertility, Male - genetics | Kidney - abnormalities | Male Urogenital Diseases - pathology | Adult | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | Male Urogenital Diseases - genetics | Gene mutations | Abnormalities | Cystic fibrosis | Genetic aspects | Birth defects | Genetic regulation | Renal agenesis | Health aspects | Vas deferens | Haplotypes | Congenital diseases | Statistical analysis | Spermatogenesis | Males | Abdomen | Genotype & phenotype | Biopsy | Infertility | Deoxyribonucleic acid--DNA | Polymorphism | Index Medicus | cystic fibrosis transmembrane conductance regulator gene | ectopic kidney | congenital absence of seminal vesicles | Original | unilateral renal agenesis | Congenital bilateral absence of vas deferens - congenital absence of seminal vesicles - cystic fibrosis transmembrane conductance regulator gene - ectopic kidney - unilateral renal agenesis
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6. Full Text CFTR Variants and Renal Abnormalities in Males With Congenital Unilateral Absence of the Vas Deferens (CUAVD): A Systematic Review and Meta-analysis of Observational Studies
by Cai, Hongcai and Qing, Xingrong and Niringiyumukiza, Jean Damascene and Zhan, Xuxin and Mo, Dunsheng and Zhou, Yuanzhong and Shang, Xuejun
Obstetrical & gynecological survey, ISSN 0029-7828, 09/2019, Volume 74, Issue 9, pp. 521 - 522
Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Complications and side effects | Abnormalities | Genetic aspects | Kidney diseases | Diagnosis | Health aspects | Genitourinary organs | Vas deferens | Risk factors | Membrane proteins
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7. Full Text Duplicated Vas Deferens Found Incidentally during Inguinal Hernia Repair
by Bailey, Kimberly Shilling and Werner, Zachary and Morris, Jessop and Rokosz, Jennifer
The American surgeon, ISSN 0003-1348, 8/2019, Volume 85, Issue 8, pp. 426 - 427
Life Sciences & Biomedicine | Surgery | Science & Technology | Hernia | Vasectomy | Fertility | Reproduction (copying) | Abnormalities | Hernias | Infertility | Bladder | Ureter | Urology | Vas deferens | Index Medicus
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8. Full Text CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies
by Cai, Hongcai and Qing, Xingrong and Niringiyumukiza, Jean Damascene and Zhan, Xuxin and Mo, Dunsheng and Zhou, Yuanzhong and Shang, Xuejun
Genetics in medicine, ISSN 1098-3600, 04/2019, Volume 21, Issue 4, pp. 826 - 836
F508del | renal abnormality | congenital unilateral absence of the vas deferens | CFTR | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Kidney - physiology | Vas Deferens - pathology | Kidney Diseases - pathology | Gene Frequency | Humans | Risk Factors | Vas Deferens - abnormalities | Genotype | Male | Male Urogenital Diseases - complications | Kidney Diseases - genetics | Kidney - abnormalities | Urogenital Abnormalities - complications | Alleles | Male Urogenital Diseases - pathology | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Kidney Diseases - complications | Male Urogenital Diseases - genetics | Urogenital Abnormalities - genetics | Systematic review | Index Medicus | 5T
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9. Imaging of the seminal vesicle and vas deferens
by Kim, Bohyun and Kawashima, Akira and Ryu, Jeong-Ah and Takahashi, Naoki and Hartman, Robert P and King, Bernard F
Radiographics, ISSN 0271-5333, 07/2009, Volume 29, Issue 4, pp. 1105 - 1121
Diagnostic Imaging - methods | Radiography | Seminal Vesicles - pathology | Vas Deferens - pathology | Diagnosis, Differential | Humans | Vas Deferens - abnormalities | Seminal Vesicles - diagnostic imaging | Vas Deferens - diagnostic imaging | Male | Seminal Vesicles - abnormalities | Genital Diseases, Male - diagnosis
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10. Full Text CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis
by Yu, Jianmin and Chen, Zhanghui and Ni, Ya and Li, Zhongxiang
Human reproduction (Oxford), ISSN 0268-1161, 1/2012, Volume 27, Issue 1, pp. 25 - 35
CFTR | systemic review and meta-analysis | CBAVD | genetic association study | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Gynecology. Andrology. Obstetrics | Biological and medical sciences | Medical sciences | Genetic Predisposition to Disease | Humans | Vas Deferens - abnormalities | Genotype | Male | Risk | Homozygote | Alleles | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Heterozygote | Mutation | Odds Ratio | Male Urogenital Diseases - genetics | Index Medicus
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11. Unilateral segmental dysplasia of the vas deferens
by Saitz, Theodore R and Thomas, Anil A
Canadian journal of urology, ISSN 1195-9479, 2018, Volume 25, Issue 6, pp. 9620 - 9622
Infertility | Vasectomy | Congenital absence of the vas deferens | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Vas Deferens - pathology | Humans | Vas Deferens - abnormalities | Adult | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Male
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12. Full Text Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens
by Patat, Olivier and Pagin, Adrien and Siegfried, Aurore and Mitchell, Valérie and Chassaing, Nicolas and Faguer, Stanislas and Monteil, Laetitia and Gaston, Véronique and Bujan, Louis and Courtade-Saïdi, Monique and Marcelli, François and Lalau, Guy and Rigot, Jean-Marc and Mieusset, Roger and Bieth, Eric
American journal of human genetics, ISSN 0002-9297, 08/2016, Volume 99, Issue 2, pp. 437 - 442
Exome - genetics | DNA Mutational Analysis | Genes, X-Linked - genetics | Pedigree | Gene Deletion | Humans | Vas Deferens - abnormalities | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Female | Male | Receptors, G-Protein-Coupled - genetics | Male Urogenital Diseases - genetics | Genotype & phenotype | Congenital diseases | Sperm | Infertility | Genomics | Mutation | Cell adhesion & migration | Index Medicus | Life Sciences | Reproductive Biology | Report
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13. Full Text Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients
by Luo, Shaoge and Feng, Jiarong and Zhang, Yanan and Yang, Xiaojian and Ma, Gongchao and Hu, Tengfei and Xi, Yu and Tu, Xuchong and Wang, Chunlin and Zhang, Hui and Zou, Zijun and Zhang, Yan
Gene, ISSN 0378-1119, 01/2021, Volume 765, pp. 145045 - 145045
CAVD | CFTR variants | Novel variants | Variant spectrum | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Gene Frequency - genetics | Humans | Vas Deferens - abnormalities | Asian Continental Ancestry Group - genetics | Exons - genetics | Male | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | DNA Mutational Analysis - methods | Mutation - genetics | Infertility, Male - genetics | Alleles | Vas Deferens - metabolism | Azoospermia - genetics | Adult | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Male Urogenital Diseases - metabolism | Male Urogenital Diseases - genetics | Index Medicus
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