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Journal Abstract Search

100 related items for PubMed ID: 7036745

  • 1. Achondrogenesis: a review with special consideration of achondrogenesis type II (Langer-Saldino).
    Chen H, Liu CT, Yang SS.
    Am J Med Genet; 1981; 10(4):379-94. PubMed ID: 7036745
    [Abstract] [Full Text] [Related]

  • 2. Achondrogenesis type II (Langer-Saldino)--a case report.
    Swar MO, Srikrishna BV.
    Afr J Med Med Sci; 1995 Sep; 24(3):297-9. PubMed ID: 8798967
    [Abstract] [Full Text] [Related]

  • 3. Antenatal diagnosis of achondrogenesis type II.
    Kodandapani S, Ramkumar V.
    JNMA J Nepal Med Assoc; 2009 Sep; 48(174):155-7. PubMed ID: 20387359
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  • 5. Achondrogenesis type II with polydactyly.
    Rittler M, Orioli IM.
    Am J Med Genet; 1995 Nov 06; 59(2):157-60. PubMed ID: 8588578
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  • 6. Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity.
    Aleck KA, Grix A, Clericuzio C, Kaplan P, Adomian GE, Lachman R, Rimoin DL.
    Am J Med Genet; 1987 Jun 06; 27(2):295-312. PubMed ID: 3605216
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  • 7. Achondrogenesis type I: delineation of further heterogeneity and identification of two distinct subgroups.
    Borochowitz Z, Lachman R, Adomian GE, Spear G, Jones K, Rimoin DL.
    J Pediatr; 1988 Jan 06; 112(1):23-31. PubMed ID: 3275766
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  • 8. [Achondrogenesis (Houston-Harris type, Langer-Saldino type, Parenti-Fraccaro type)].
    Matsuo M.
    Ryoikibetsu Shokogun Shirizu; 2001 Jan 06; (33):90-1. PubMed ID: 11462732
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  • 10. Achondrogenesis: new nosology with evidence of genetic heterogeneity.
    Whitley CB, Gorlin RJ.
    Radiology; 1983 Sep 06; 148(3):693-8. PubMed ID: 6878687
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  • 11. Case report 122: lethal short-limbed dwarfism: achondrogenesis type 2 (Fraccaro-Langer-Saldino).
    Dorfman HD, Lorenzo J.
    Skeletal Radiol; 1980 Sep 06; 5(3):189-92. PubMed ID: 6970987
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  • 13. [New subtype of familial achondrogenesis type IA (Houston-Harris)].
    Ramírez-García SA, García-Cruz D, Cervantes-Aragón I, Bitar-Alatorre WE, Dávalos-Rodríguez IP, Dávalos-Rodríguez NO, Corona-Rivera JR, Sánchez-Corona J.
    Cir Cir; 2018 Sep 06; 86(1):89-98. PubMed ID: 29681641
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  • 14. Achondrogenesis II-hypochondrogenesis: variability versus heterogeneity.
    Borochowitz Z, Ornoy A, Lachman R, Rimoin DL.
    Am J Med Genet; 1986 Jun 06; 24(2):273-88. PubMed ID: 3717210
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  • 15. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP, Moerman P.
    Genet Couns; 1998 Jun 06; 9(1):61-2. PubMed ID: 9555592
    [No Abstract] [Full Text] [Related]

  • 16. [Sex chromosome abnormality: report of three clinical cases of X pentasomy].
    Biroli E, Ghimenti C, Ricci I, Pirola B, Liverani ME, Perona A, Galligani L, Guala A, Angeli G.
    Pathologica; 2003 Dec 06; 95(6):444-6. PubMed ID: 15080523
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  • 18. [Lethal osteo-chondro-dysplasia: feto-pathological study of 32 cases].
    Lahmar-Boufaroua A, Yacoubi MT, Hmisssa S, Selmi M, Korbi S.
    Tunis Med; 2009 Feb 06; 87(2):127-32. PubMed ID: 19522446
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