203 related articles for article (PubMed ID: 1283287)
1. Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay.
Davee MA; Moore CA; Bull MJ; Hodes ME
Am J Med Genet; 1992 Oct; 44(3):293-6. PubMed ID: 1283287
[TBL] [Abstract][Full Text] [Related]
2. Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay: a 4p deletion?
de Die-Smulders C; Schrander-Stumpel C; Fryns JP
Am J Med Genet; 1993 Nov; 47(6):936. PubMed ID: 7506486
[No Abstract] [Full Text] [Related]
3. 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; 47(4):494-503. PubMed ID: 8256813
[TBL] [Abstract][Full Text] [Related]
4. The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patients.
Hershkovitz E; Shalitin S; Levy J; Leiberman E; Weinshtock A; Varsano I; Gorodischer R
Isr J Med Sci; 1995 May; 31(5):293-7. PubMed ID: 7538982
[TBL] [Abstract][Full Text] [Related]
5. Acrocallosal syndrome in two African brothers born to consanguineous parents.
Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS
Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201
[TBL] [Abstract][Full Text] [Related]
6. Mild growth retardation and developmental delay, microcephaly, and a distinctive facial appearance.
Partington M; Anderson D
Am J Med Genet; 1994 Jan; 49(2):247-50. PubMed ID: 7509568
[TBL] [Abstract][Full Text] [Related]
7. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
Froster UG; Rehder H; Höhn W; Oberheuser F
Am J Med Genet; 1993 Oct; 47(5):717-22. PubMed ID: 8267003
[TBL] [Abstract][Full Text] [Related]
8. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
Smith AC; McGavran L; Robinson J; Waldstein G; Macfarlane J; Zonona J; Reiss J; Lahr M; Allen L; Magenis E
Am J Med Genet; 1986 Jul; 24(3):393-414. PubMed ID: 2425619
[TBL] [Abstract][Full Text] [Related]
9. [Cerebro-hepato-renal syndrome. Apropos of a new case].
García Burriel JI; Carbajosa Herrero MT; Pedraz García C; Santos Borbujos J; Mateos Cañizal M; García González P
An Esp Pediatr; 1986 Jul; 25(1):67-9. PubMed ID: 3752742
[No Abstract] [Full Text] [Related]
10. [Craniofacial dysmorphism with flexion of the fingers. Marden-Walker syndrome? (author's transl)].
Kubryk N; Borde M
Ann Pediatr (Paris); 1982 Mar; 29(3):208-10. PubMed ID: 6177274
[No Abstract] [Full Text] [Related]
11. [Pena-Shokeir syndrome: report of a case with benign outcome].
Romeo MG; Betta P; Rodonò A; Tina LG; Distefano G
Pediatr Med Chir; 1995; 17(1):73-5. PubMed ID: 7739933
[TBL] [Abstract][Full Text] [Related]
12. [Acceleration of bone maturation and dysmorphic syndrome in 2 siblings (Marshall-Weaver syndrome)].
Jalaguier J; Montoya F; Germain M; Bonnet H
J Genet Hum; 1983 Dec; 31 Suppl 5():385-95. PubMed ID: 6674414
[TBL] [Abstract][Full Text] [Related]
13. Müllerian duct abnormalities and galactosaemia heterozygosity: report of a family.
Aughton DJ
Clin Dysmorphol; 1993 Jan; 2(1):55-61. PubMed ID: 8298739
[TBL] [Abstract][Full Text] [Related]
14. Toriello-Carey syndrome: report of a new case.
Camera G; Righi E; Romagnoli G
Clin Dysmorphol; 1993 Jul; 2(3):260-3. PubMed ID: 7506967
[TBL] [Abstract][Full Text] [Related]
15. [A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"].
Fryns JP; Moerman P; Van den Berghe H; Aymé S
J Genet Hum; 1989 Sep; 37(3):203-5. PubMed ID: 2625623
[TBL] [Abstract][Full Text] [Related]
16. Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?
Chitayat D; Haj-Chahine S; Stalker HJ; Azouz EM; Côté A; Halal F
Am J Med Genet; 1993 Jan; 45(1):1-4. PubMed ID: 8418638
[TBL] [Abstract][Full Text] [Related]
17. [Robinow's syndrome associated with deafness].
Samoud A; Menif K; Boulaares M; Ben Dridi MF
Arch Fr Pediatr; 1993 Dec; 50(10):897-9. PubMed ID: 8053771
[TBL] [Abstract][Full Text] [Related]
18. Craniofacial pattern profile (CFPP) evaluation of facial dysmorphology in a familial syndrome with corneal anesthesia and multiple congenital anomalies.
Saksena SS; Ramos-Arroyo MA; Hodes ME
Am J Phys Anthropol; 1987 Dec; 74(4):465-71. PubMed ID: 3442298
[TBL] [Abstract][Full Text] [Related]
19. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
[TBL] [Abstract][Full Text] [Related]
20. Fryns syndrome: another example of non-lethal outcome with severe mental handicap.
Hanssen AM; Schrander-Stumpel CT; Thiry PA; Fryns JP
Genet Couns; 1992; 3(4):187-93. PubMed ID: 1472353
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
