91 related articles for article (PubMed ID: 1264532)
1. [Syndrome of multiple abnormalities in a 4-year-old girl].
Jankowski A; Pawlaczyk B
Pediatr Pol; 1976 Apr; 51(4):449-51. PubMed ID: 1264532
[No Abstract] [Full Text] [Related]
2. [Pectoral aplasia and Poland's syndrome].
Eriksen S
Nord Med; 1970 Mar; 83(12):357-61. PubMed ID: 5424751
[No Abstract] [Full Text] [Related]
3. [Coffin-Siris syndrome in a 5-year-old girl].
Meinecke P; Engelbrecht R; Schaefer E
Monatsschr Kinderheilkd; 1986 Sep; 134(9):692-5. PubMed ID: 3785238
[TBL] [Abstract][Full Text] [Related]
4. [Clinical and genetic analysis of the Townes-Brocks syndrome].
Il'ina EG; Laziuk GI
Tsitol Genet; 1992; 26(4):32-5. PubMed ID: 1440915
[TBL] [Abstract][Full Text] [Related]
5. [Klippel-Feil syndrome associated with renal agenesia and heart defect in an 11-year-old girl].
Krawczyński M; Spiller R; Borski K
Wiad Lek; 1983 Sep; 36(18):1527-31. PubMed ID: 6666133
[No Abstract] [Full Text] [Related]
6. [Holt-Oram syndrome in a 11-year-old girl with hemiatrophy of the body].
Kozlowski K; Januś S; Popczyńska-Markowa M
Pediatr Pol; 1970 Feb; 45(2):221-7. PubMed ID: 5437025
[No Abstract] [Full Text] [Related]
7. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father.
Ioan DM; Dagomiz D; Fryns JP
Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221
[TBL] [Abstract][Full Text] [Related]
8. [Carpenter's syndrome in an 11-year-old girl].
Bartkowiak K; Piontek E; Pawlaczyk B
Pediatr Pol; 1972; 47(3):349-51. PubMed ID: 5019700
[No Abstract] [Full Text] [Related]
9. S--the whistling-face syndrome: report of a case with a renal anomaly.
Hashemi C; Mahloudji M
Birth Defects Orig Artic Ser; 1974; 10(5):265-7. PubMed ID: 4220008
[No Abstract] [Full Text] [Related]
10. Silver's syndrome with unusual presentations.
Kapoor KL; Ahmad S; Karihalu PL; Ishar K
J Indian Med Assoc; 1984 Nov; 82(11):408-10. PubMed ID: 6543559
[No Abstract] [Full Text] [Related]
11. New syndrome: a digito-reno-cerebral syndrome.
Eronen M; Somer M; Gustafsson B; Holmberg C
Am J Med Genet; 1985 Oct; 22(2):281-5. PubMed ID: 4050858
[No Abstract] [Full Text] [Related]
12. [Amplification of the clinical spectrum of the Robinow syndrome].
González de Dios J; Moya Benavent M
An Esp Pediatr; 1998 Feb; 48(2):167-9. PubMed ID: 9577026
[No Abstract] [Full Text] [Related]
13. [Schwartz-Jampel syndrome type 2 versus Stüve-Wiedemann syndrome].
Navarrete Faubel FE; Pérez Aytés A; Pastor Rosado J; Mascarell Gregoria A
An Esp Pediatr; 2002 May; 56(5):473-4. PubMed ID: 12042125
[No Abstract] [Full Text] [Related]
14. [Radial-renal-ocular syndrome].
Kurosawa K
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):563-4. PubMed ID: 11528897
[No Abstract] [Full Text] [Related]
15. [Aarskog syndrome. A case report].
Cincinnati P; Lombardi AM; Morelli M; Rutiloni C
Minerva Pediatr; 1994 Sep; 46(9):407-10. PubMed ID: 7799889
[TBL] [Abstract][Full Text] [Related]
16. Tricho-rhino-phalangeal syndrome type I.
Eroğlu Y; Erçal D
Turk J Pediatr; 1996; 38(4):537-42. PubMed ID: 8993187
[TBL] [Abstract][Full Text] [Related]
17. [Case of leprechaunism in a girl].
Badalian LO; Petrukhin AS; Filina NP
Pediatriia; 1980 Dec; (12):24-7. PubMed ID: 7220166
[No Abstract] [Full Text] [Related]
18. [The MMT syndrome (microcephaly, mesobrachyphalangy and tracheoesophageal fistula). The first case described in Spain and a review of the literature].
Martínez-Frías ML; Blanco García M; Urioste Azcorra M; Rodríguez Pinilla E; Villa Milla A
An Esp Pediatr; 1996 Jul; 45(1):87-9. PubMed ID: 8849141
[No Abstract] [Full Text] [Related]
19. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Hsia YE; Bratu M; Herbordt A
Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860
[No Abstract] [Full Text] [Related]
20. Lacrimo-auriculo-dento-digital syndrome. Case report, review of the literature, and clinical spectrum.
Lehotay M; Kunkel M; Wehrbein H
J Orofac Orthop; 2004 Sep; 65(5):425-32. PubMed ID: 15378197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]