169 related articles for article (PubMed ID: 4462626)
1. Elucidation of a 'new' pleiotropic connective tissue disorder.
Welch JP
Birth Defects Orig Artic Ser; 1974; 10(10):138-46. PubMed ID: 4462626
[No Abstract] [Full Text] [Related]
2. M--craniocarpotarsal dystrophy (whistling face syndrome) in two families.
Jorgenson RJ
Birth Defects Orig Artic Ser; 1974; 10(5):237-42. PubMed ID: 4220006
[No Abstract] [Full Text] [Related]
3. Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?
Frank Y; Ziprkowski M; Romano A; Stein R; Katznelson MB; Cohen B; Goodman RM
J Genet Hum; 1973 Jun; 21(2):67-72. PubMed ID: 4805907
[No Abstract] [Full Text] [Related]
4. The Greig cephalopolysyndactyly syndrome in a Canadian family.
Chudley AE; Houston CS
Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
[No Abstract] [Full Text] [Related]
5. Gastro-cutaneous syndrome: peptic ulcer/hiatal hernia, multiple lentigines/café-au-lait spots, hypertelorism, and myopia.
Halal F; Gervais MH; Baillargeon J; Lesage R
Am J Med Genet; 1982 Feb; 11(2):161-76. PubMed ID: 7065007
[TBL] [Abstract][Full Text] [Related]
6. [Greig's syndrome or Pehu's essential hypertelorism syndrome].
Giovannucci Uzielli ML; Bettini F; Carattoli MT; Maffei G
Minerva Pediatr; 1979 Jul; 31(13):1015-22. PubMed ID: 481368
[No Abstract] [Full Text] [Related]
7. A familial syndrome of short stature associated with facial dysplasia and genital anomalies.
Aarskog D
J Pediatr; 1970 Nov; 77(5):856-61. PubMed ID: 5504078
[No Abstract] [Full Text] [Related]
8. [Aarskog's genito-digito-facial syndrome].
Fouanon C; André MJ; Gillot F
Bull Soc Ophtalmol Fr; 1976 Nov; 76(11):981-5. PubMed ID: 1030364
[No Abstract] [Full Text] [Related]
9. [Pyknodysostosis. Review and report of 6 cases].
Nielsen EL
Ugeskr Laeger; 1973 Sep; 135(39):2093-8. PubMed ID: 4590079
[No Abstract] [Full Text] [Related]
10. Fetal face syndrome with acral dysostosis.
Schinzel A; Zellweger H; Grella A; Prader A
Helv Paediatr Acta; 1974 Apr; 29(1):55-60. PubMed ID: 4838165
[No Abstract] [Full Text] [Related]
11. [Aarskog syndrome (author's transl)].
Kunze J; Spranger J
Klin Padiatr; 1973 Nov; 185(6):490-4. PubMed ID: 4798676
[No Abstract] [Full Text] [Related]
12. The Aarskog syndrome in three brothers.
Funderburk SJ; Crandall BF
Clin Genet; 1974; 6(2):119-24. PubMed ID: 4430151
[No Abstract] [Full Text] [Related]
13. Two new familial cases of the G syndrome.
Frias JL; Rosenbloom AL
Birth Defects Orig Artic Ser; 1975; 11(2):54-7. PubMed ID: 1227574
[No Abstract] [Full Text] [Related]
14. [Faciodigitogenital (Aarskog-Scott) syndrome].
Fragoso R; García-Cruz D; Sánchez-Corona J; Nazará Z; Cantú JM
Bol Med Hosp Infant Mex; 1982 Apr; 39(4):291-5. PubMed ID: 7093037
[No Abstract] [Full Text] [Related]
15. [The G syndrome: description of a case/and familial studies].
Calandi C; Adami-Lami Conti C; Mannini A; Fantacci C; Nistri R; Giovannucci ML
Arch De Vecchi Anat Patol; 1980; 64(1):59-73. PubMed ID: 7027970
[No Abstract] [Full Text] [Related]
16. [Familial and hereditary microcephaly. Study of 10 cases in 4 families].
Bost M; Crouzet G; Jalbert P; Lesage A; Beaudoing A
Pediatrie; 1971 Sep; 26(6):587-98. PubMed ID: 5116340
[No Abstract] [Full Text] [Related]
17. [The Greig syndrome].
Fehlow P
Kinderarztl Prax; 1984 Mar; 52(3):145-9. PubMed ID: 6727153
[No Abstract] [Full Text] [Related]
18. G--polysyndactyly in an Egyptian family.
Temtamy SA; Lontly AH
Birth Defects Orig Artic Ser; 1974; 10(5):207-15. PubMed ID: 4469988
[No Abstract] [Full Text] [Related]
19. [Family with Crouzon's craniofacial dysostosis].
Vaillaud JC; Manassero J; Badach L
J Genet Hum; 1974 Dec; 22(4):381-7. PubMed ID: 4461765
[No Abstract] [Full Text] [Related]
20. [Three new cases of Meckel's syndrome or Gruber's splanchnocystic dysencephaly in siblings. Anatomo-pathologic and cytogenetic study. Nosologic discussion].
Naffah J; Ghosn G; Gharios N
Arch Fr Pediatr; 1972 Dec; 29(10):1069-81. PubMed ID: 4662280
[No Abstract] [Full Text] [Related]
[Next] [New Search]
