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Items: 1 to 20 of 143

1.

Bilateral multicystic renal dysplasia with potter sequence. A case with penile agenesis.

Dursun A, Ermis B, Numanoglu V, Bahadir B, Seckiner I.

Saudi Med J. 2006 Nov;27(11):1745-7.

PMID:
17106555
2.

[Potter sequence in a neonate with bilateral renal dysplasia with genetic aspects].

Dyrek I, Gajda B, Osuch-Jaczewska R, Gruszka L, Mocny J, Gaida H, Trzesiok K, Pogorzelec B, Pilch-Kucia H, Mańka B.

Wiad Lek. 2001;54(3-4):219-23. Polish.

PMID:
11436690
3.
4.

Potter sequence complicated by congenital cystic lesion of the bladder.

Abe Y, Mizuno K, Horie H, Matsumoto M, Yamaoka A, Mizutani K, Takeuchi T, Iikura Y.

Am J Perinatol. 2002 Jul;19(5):267-72.

PMID:
12152145
5.

Penile agenesis complicated by Potter sequence.

Arai M, Suzuki S, Ishino H, Igarashi K, Araki T.

Arch Gynecol Obstet. 2001 Nov;265(4):219-20.

PMID:
11789751
6.

Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardation.

Cormier-Daire V, Chauvet ML, Lyonnet S, Briard ML, Munnich A, Le Merrer M.

J Med Genet. 2000 Jul;37(7):520-4.

7.

Syndromic ear anomalies and renal ultrasounds.

Wang RY, Earl DL, Ruder RO, Graham JM Jr.

Pediatrics. 2001 Aug;108(2):E32.

PMID:
11483842
8.

Management dilemmas in patients with hereditary renal adysplasia.

Morava E, Smith C, Pierce M, Andersson HC.

J La State Med Soc. 2001 Jan;153(1):27-30.

PMID:
11272448
9.

A rare case of aphallia with right kidney hypoplasia and left kidney dysplasia.

Aslanabadi S, Zarrintan S, Abdollahi H, Rikhtegar R, Beheshtirouy S, Badebarin D, Baky Fahmy MA.

Arch Iran Med. 2015 Apr;18(4):257-9. doi: 015184/AIM.0013. Review.

10.

[Hereditary renal agenesis . Report of a case].

Stella A.

Minerva Ginecol. 1998 Jun;50(6):255-9. Italian.

PMID:
9763817
11.

Congenital absence of penis.

Roth JK Jr, Marshall RH, Angel JR, Daftary M, Lewis RW.

Urology. 1981 Jun;17(6):579-83.

PMID:
7245449
12.

Bladder agenesis in a male neonate.

Patkowski D, Apoznański W, Szydełko T, Jaworski W, Smigiel R.

J Pediatr Surg. 2008 Nov;43(11):e1-3. doi: 10.1016/j.jpedsurg.2008.06.003.

PMID:
18970912
13.

Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report.

Acién P, Galán F, Manchón I, Ruiz E, Acién M, Alcaraz LA.

Orphanet J Rare Dis. 2010 Apr 14;5:6. doi: 10.1186/1750-1172-5-6.

14.

Aphallia, lung agenesis and multiple defects of blastogenesis.

Gérard-Blanluet M, Lambert V, Khung-Savatovsky S, Perrin-Sabourin L, Passemard S, Baumann C, Delezoide AL, Verloes A.

Fetal Pediatr Pathol. 2011;30(1):22-6. doi: 10.3109/15513815.2010.494698.

PMID:
21204662
15.

VACTERL association with a rare vertebral anomaly (butterfly vertebra) in a case of monochorionic twin.

Sandal G, Aslan N, Duman L, Ormeci AR.

Genet Couns. 2014;25(2):231-5.

PMID:
25059024
16.

[Pathological study of the kidney and the lung in patients with Potter sequence].

Shimada K, Hosokawa S, Matsumoto F, Matsumoto S.

Nihon Hinyokika Gakkai Zasshi. 1997 Jul;88(7):664-9. Japanese.

17.

Renal multicystic dysplasia: an occasional manifestation of the hereditary renal adysplasia syndrome.

Squiers EC, Morden RS, Bernstein J.

Am J Med Genet Suppl. 1987;3:279-84.

PMID:
3130862
18.
19.

Agenesis of the penis: patterns of associated malformations.

Evans JA, Erdile LB, Greenberg CR, Chudley AE.

Am J Med Genet. 1999 May 7;84(1):47-55.

PMID:
10213046
20.

Pulmonary agenesis as part of the VACTERL sequence.

Knowles S, Thomas RM, Lindenbaum RH, Keeling JW, Winter RM.

Arch Dis Child. 1988 Jul;63(7 Spec No):723-6.

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