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Items: 1 to 20 of 102

1.
2.

Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndrome.

Bialer MG, Penchaszadeh VB, Kahn E, Libes R, Krigsman G, Lesser ML.

Am J Med Genet. 1987 Nov;28(3):723-31. Review.

PMID:
3322011
3.

[Genital tract anomalies in anorectal malformations].

Sauvage P, Bientz J, Leculée R, Elahi B.

Chir Pediatr. 1986;27(5):305-8. French.

PMID:
3815661
4.

Duplication of the müllerian ducts and genitourinary malformations. Part II: analysis of malformations.

Gilsanz V, Cleveland RH, Reid BS.

Radiology. 1982 Sep;144(4):797-801.

PMID:
6213980
5.

A newly recognized dwarfing syndrome.

Robinow M, Silverman FN, Smith HD.

Am J Dis Child. 1969 Jun;117(6):645-51. No abstract available.

PMID:
5771504
6.

Phocomelia, ectrodactyly, skull defect and urinary system anomaly: Schinzel-phocomelia syndrome?

Evliyaoğlu N, Temoçin AK, Altintaş DU, Duman N, Satar N, Süleymanova D.

Clin Genet. 1996 Feb;49(2):70-3.

PMID:
8740915
7.

[Limb, upper hypoplasia-müllerian duct defects].

Chinen Y.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):98. Review. Japanese. No abstract available.

PMID:
11529064
8.
9.

Acrofacial dysostosis with ambiguous genitalia.

Wulfsberg EA, Curtis J, Wiswell TE, Puntel RA, Levin SW.

Am J Med Genet. 1990 Nov;37(3):384-7.

PMID:
2260569
10.

Visceral anomalies in the Meckel syndrome.

Rapola J, Salonen R.

Teratology. 1985 Apr;31(2):193-201.

PMID:
3992488
11.
12.

Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.

Halal F, Homsy M, Perreault G.

Am J Med Genet. 1984 Apr;17(4):753-62.

PMID:
6426304
13.

Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency.

Schönau E, Pfeiffer RA, Schweikert HU, Böwing B, Schott G.

Eur J Pediatr. 1990 Jun;149(9):615-7.

PMID:
2373109
14.

An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomalies.

Verma IC, Bhargava S, Agarwal S.

Birth Defects Orig Artic Ser. 1975;11(6):167-74. Review. No abstract available.

PMID:
1103993
15.
16.

Müllerian anomalies and renal agenesis: autosomal dominant urogenital adysplasia.

Biedel CW, Pagon RA, Zapata JO.

J Pediatr. 1984 Jun;104(6):861-4.

PMID:
6726517
17.

Syndrome of polydactyly, micromelia, genital hypoplasia and respiratory distress (Majewski syndrome).

Passarge E.

Birth Defects Orig Artic Ser. 1975;11(2):464-5. No abstract available.

PMID:
1227571
18.

Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies.

Urioste M, Rodríguez JI, Barcia JM, Martín M, Escribá R, Pardo M, Camino J, Martínez-Frías ML.

Am J Med Genet. 1993 Sep 15;47(4):494-503.

PMID:
8256813
19.

Pseudo-trisomy 13 syndrome with upper limb shortness and radial hypoplasia.

Boles RG, Teebi AS, Neilson KA, Meyn MS.

Am J Med Genet. 1992 Nov 15;44(5):638-40.

PMID:
1481825
20.

[Robinow's syndrome].

Nájera-Martínez P, Gómez-Valencia L, Váldes-Bravo JL.

Bol Med Hosp Infant Mex. 1988 Aug;45(8):537-42. Review. Spanish. No abstract available.

PMID:
3052496

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