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Items: 1 to 20 of 112

1.

The Schinzel syndrome in a mother and daughter.

Hecht JT, Scott CI Jr.

Clin Genet. 1984 Jan;25(1):63-7. No abstract available.

PMID:
6538465
2.

Oligomeganephronia with covered anus in twins.

Mansour A, Reye RD, Roy LP.

Aust Paediatr J. 1977 Sep;13(3):187-92. No abstract available.

PMID:
565200
3.

The ulnar-mammary syndrome: an autosomal dominant pleiotropic gene.

Schinzel A, Illig R, Prader A.

Clin Genet. 1987 Sep;32(3):160-8. Erratum in: Clin Genet 1987 Dec;32(6):425.

PMID:
3621662
4.
5.

Clinical variability in acro-cardio-facial-syndrome.

Kariminejad A, Bozorgmehr B, Sedighi Gilani MA, Almadani N, Kariminejad MH.

Am J Med Genet A. 2008 Aug 1;146A(15):1977-9. doi: 10.1002/ajmg.a.32052.

PMID:
18627040
6.

Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomalies.

Lukusa T, Moerman P, Fryns JP.

Genet Couns. 1996;7(3):207-12.

PMID:
8897042
7.

Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies.

Townes PL, Brocks ER.

J Pediatr. 1972 Aug;81(2):321-6. No abstract available.

PMID:
5042490
8.

[Concordant cases of renal agenesis and a caudal regressive anomalad in monozygotic twins].

Métneki J.

Orv Hetil. 1982 Nov 28;123(48):2959-61. Hungarian. No abstract available.

PMID:
6891450
9.

A syndrome of multiple congenital malformations with absent external genitalia, urethral and anal openings in one of twins.

Sinniah D, Manuel JK.

Singapore Med J. 1980 Apr;21(2):534-6. No abstract available.

PMID:
7190327
10.

Imperforate anus in Feingold syndrome.

Büttiker V, Wojtulewicz J, Wilson M.

Am J Med Genet. 2000 May 29;92(3):166-9.

PMID:
10817649
11.

D1 ring chromosome in newborn with peculiar face, polydactyly, imperforate anus, arrhinencephaly, and other malformations.

Biles AR Jr, Lüers T, Sperling K.

J Med Genet. 1970 Dec;7(4):399-401. No abstract available.

12.

Twin births and genetic counseling.

Lowry RB.

Obstet Gynecol. 1972 Sep;40(3):452-3. No abstract available.

PMID:
5066330
13.

Autosomal recessive type of whistling face syndrome in twins.

Kousseff BG, McConnachie P, Hadro TA.

Pediatrics. 1982 Mar;69(3):328-31.

PMID:
7199706
14.

Pfeiffer type cardiocranial syndrome: a third case report.

Williamson-Kruse L, Biesecker LG.

J Med Genet. 1995 Nov;32(11):901-3. Review.

15.

[Role of heredity in the origin of developmental defects].

Brunecký Z.

Cesk Pediatr. 1968 May;23(5):435-7. Czech. No abstract available.

PMID:
5660454
16.

Weyers' ulnar ray/oligodactyly syndrome.

Lungarotti MS, Calabro A.

J Med Genet. 1993 Jun;30(6):533. No abstract available.

17.

Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome.

Franceschini P, Vardeu MP, Dalforno L, Signorile F, Franceschini D, Lala R, Matarazzo P.

Am J Med Genet. 1992 Dec 1;44(6):807-12. Review.

PMID:
1481852
18.

Familial Williams syndrome.

Cortada X, Taysi K, Hartmann AF.

Clin Genet. 1980 Sep;18(3):173-6.

PMID:
7192194
19.

[Two unusual forms of pyloric hypertrophic stenosis: late onset form and familial form in dizygote twins].

Masson P, Quetin P, Es Sathi A, Tizeggaghine A, Touati K, De Luca JL.

Arch Pediatr. 2002 Sep;9(9):973-4. French. No abstract available.

PMID:
12387181
20.

[Anal atresia in twins].

Tünte W.

Z Kinderheilkd. 1969;106(1):21-32. German. No abstract available.

PMID:
5801234

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