These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 8076412)

  • 21. Congenital heart defects in Aarskog syndrome.
    Fernandez I; Tsukahara M; Mito H; Yoshii H; Uchida M; Matsuo K; Kajii T
    Am J Med Genet; 1994 May; 50(4):318-22. PubMed ID: 8209909
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Structural central nervous system (CNS) anomalies in Kabuki syndrome.
    Ben-Omran T; Teebi AS
    Am J Med Genet A; 2005 Aug; 137(1):100-3. PubMed ID: 16007616
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome).
    Koppe R; Kaplan P; Hunter A; MacMurray B
    Am J Med Genet; 1989 Nov; 34(3):305-12. PubMed ID: 2596519
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Undiagnosed syndrome of psychomotor retardation, low birthweight dwarfism, skeletal, dental, dermal and genital anomalies.
    Elliott DE
    Birth Defects Orig Artic Ser; 1975; 11(2):364-7. PubMed ID: 1241660
    [No Abstract]   [Full Text] [Related]  

  • 26. Aarskog syndrome associated with hypermetropia and toe anomaly.
    Caksen H; Kurtoğlu S; Ciftçi A; Cağil N; Gikrikçi V
    S Afr Med J; 1997 Dec; 87(12):1699-700. PubMed ID: 9497838
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. Rubinstein-Taybi's syndrome-a case report.
    Fukunaga N; Suda S; Ebihara Y; Laovoravit N; Laovoravit M
    Acta Pathol Jpn; 1969 Nov; 19(4):501-10. PubMed ID: 5396117
    [No Abstract]   [Full Text] [Related]  

  • 29. Aarskog syndrome: report of a family with review and discussion of nosology.
    Teebi AS; Rucquoi JK; Meyn MS
    Am J Med Genet; 1993 Jun; 46(5):501-9. PubMed ID: 8322809
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital hypothyroidism in Young-Simpson syndrome.
    Stagi S; Bindi G; Lapi E; Giovannucci-Uzielli ML; Salti R; Chiarelli F
    J Pediatr Endocrinol Metab; 2008 Nov; 21(11):1089-92. PubMed ID: 19189705
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New autosomal recessive faciodigitogenital syndrome.
    Teebi AS; Naguib KK; Al-Awadi S; Al-Saleh QA
    J Med Genet; 1988 Jun; 25(6):400-6. PubMed ID: 3398008
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Additional anomalies in 2 children with the VACTERL association].
    Arrigo T; Pandullo E; Tedeschi A; Sindoni A; Manganaro R; De Luca F
    Minerva Pediatr; 1984 Jul; 36(13-14):713-8. PubMed ID: 6150426
    [No Abstract]   [Full Text] [Related]  

  • 33. Aarskog syndrome: new oral-facial findings.
    Melnick M; Shields ED
    Clin Genet; 1976 Jan; 9(1):20-4. PubMed ID: 1248161
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene.
    Orrico A; Galli L; Faivre L; Clayton-Smith J; Azzarello-Burri SM; Hertz JM; Jacquemont S; Taurisano R; Arroyo Carrera I; Tarantino E; Devriendt K; Melis D; Thelle T; Meinhardt U; Sorrentino V
    Am J Med Genet A; 2010 Feb; 152A(2):313-8. PubMed ID: 20082460
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Redefining the genital abnormality in the Robinow syndrome. -004.
    Wilcox DT; Quinn FM; Ng CS; Dicks-Mireaux C; Mouriquand PD
    J Urol; 1997 Jun; 157(6):2312-4. PubMed ID: 9146662
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. The radiology of Coffin-Lowry syndrome.
    Padley S; Hodgson SV; Sherwood T
    Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
    [No Abstract]   [Full Text] [Related]  

  • 38. Sotos syndrome.
    Cole TR; Hughes HE
    J Med Genet; 1990 Sep; 27(9):571-6. PubMed ID: 2231650
    [No Abstract]   [Full Text] [Related]  

  • 39. Unique skeletal manifestations in patients with Primrose syndrome.
    Arora V; Leon E; Diaz J; Hove HB; Carvalho DR; Kurosawa K; Nishimura N; Nishimura G; Saxena R; Ferreira C; Puri RD; Verma IC
    Eur J Med Genet; 2020 Aug; 63(8):103967. PubMed ID: 32473227
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Orthodontic treatment of a case of Aarskog syndrome.
    Batra P; Kharbanda OP; Duggal R; Reddy P; Parkash H
    J Clin Pediatr Dent; 2003; 27(3):229-33. PubMed ID: 12739682
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.