183 related articles for article (PubMed ID: 7211953)
1. Short stature, psychomotor retardation, and unusual facial appearance in two brothers.
Smith RD; Fineman RM; Myers GG
Am J Med Genet; 1980; 7(1):5-9. PubMed ID: 7211953
[TBL] [Abstract][Full Text] [Related]
2. The neurofaciodigitorenal (NFDR) syndrome.
Freire-Maia N; Pinheiro M; Opitz JM
Am J Med Genet; 1982 Mar; 11(3):329-36. PubMed ID: 7081297
[TBL] [Abstract][Full Text] [Related]
3. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
Brooks SS; Wisniewski K; Brown WT
Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
[TBL] [Abstract][Full Text] [Related]
4. Severe mental retardation, cataracts, short stature, and primary hypogonadism in two brothers.
Martsolf JT; Hunter AG; Haworth JC
Am J Med Genet; 1978; 1(3):291-9. PubMed ID: 677168
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 5: delineation of clinical features.
DiLiberti JH; McKean R; Webb MJ; Williams G
Birth Defects Orig Artic Ser; 1977; 13(3C):185-94. PubMed ID: 890110
[TBL] [Abstract][Full Text] [Related]
6. Smith-Fineman-Myers syndrome: report of a third case.
Stephenson LD; Johnson JP
Am J Med Genet; 1985 Oct; 22(2):301-4. PubMed ID: 4050861
[TBL] [Abstract][Full Text] [Related]
7. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ
Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
[TBL] [Abstract][Full Text] [Related]
8. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH
Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066
[TBL] [Abstract][Full Text] [Related]
9. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
Bindewald B; Ulmer H; Müller U
Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348
[TBL] [Abstract][Full Text] [Related]
10. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.
Hurst JA; Baraitser M; Winter RM
Am J Med Genet; 1987 Dec; 28(4):965-70. PubMed ID: 3688035
[TBL] [Abstract][Full Text] [Related]
11. Pitt-Rogers-Danks syndrome: further delineation.
Lizcano-Gil LA; García-Cruz D; García-Cruz O; Sánchez-Corona J
Am J Med Genet; 1995 Feb; 55(4):420-2. PubMed ID: 7762580
[TBL] [Abstract][Full Text] [Related]
12. Brief clinical report: the Dubowitz syndrome in a teenager.
Fryns JP; Fabry G; Willemyns F; Van Den Berghe H
Am J Med Genet; 1979; 4(4):345-7. PubMed ID: 575467
[TBL] [Abstract][Full Text] [Related]
13. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
Thompson EM; Winter RM
Am J Med Genet; 1988 Jul; 30(3):719-24. PubMed ID: 3055984
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome.
Halal F; Gledhill R; Dudkiewicz A
Am J Med Genet; 1989 Jul; 33(3):376-81. PubMed ID: 2801772
[TBL] [Abstract][Full Text] [Related]
15. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH
Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045
[TBL] [Abstract][Full Text] [Related]
16. Trisomy of the short arm of chromosome 4: the changing phenotype with age.
Kleczkowska A; Fryns JP; van den Berghe H
Ann Genet; 1992; 35(4):217-23. PubMed ID: 1296518
[TBL] [Abstract][Full Text] [Related]
17. Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?
Pitt DB; Rogers JG; Danks DM
Am J Med Genet; 1984 Oct; 19(2):307-13. PubMed ID: 6542309
[TBL] [Abstract][Full Text] [Related]
18. Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation.
Morillo-Cucci G; Passarge E; Simpson JL; Chaganti RS; German J
Birth Defects Orig Artic Ser; 1975; 11(2):380-3. PubMed ID: 1227554
[No Abstract] [Full Text] [Related]
19. Direct transmission of the 18q- syndrome from mother to daughter.
Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W
Genet Couns; 2006; 17(2):185-9. PubMed ID: 16970036
[TBL] [Abstract][Full Text] [Related]
20. [Microencephalic nanism, severe retardation, hypertonia, obesity, and hypogonadism in two brothers: a new syndrome?].
Delozier-Blanchet CD; Haenggeli CA; Engel E
J Genet Hum; 1989 Dec; 37(4-5):353-65. PubMed ID: 2635712
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
