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9 in total

1. A FAMILIAL SYNDROME OF FACIAL AND SKELETAL ANOMALIES ASSOCIATED WITH GENITAL ABNORMALITY IN THE MALE AND NORAML GENITALS IN THE FEMALE: ANOTHER CAUSE OF MALE PSEUDOHERMAPHRODITISM.

Authors: L PINSKY; A M DIGEORGE
Journal: J Pediatr Date: 1965-06 Impact factor: 4.406

2. A CASE OF THE SMITH-LEMLI-OPITZ SYNDROME OF MULTIPLE CONGENITAL ANOMALIES IN ASSOCIATION WITH DYSPLASIA EPIPHYSIALIS PUNCTATA.

Authors: R GIBSON
Journal: Can Med Assoc J Date: 1965-03-13 Impact factor: 8.262

3. A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.

Authors: D W SMITH; L LEMLI; J M OPITZ
Journal: J Pediatr Date: 1964-02 Impact factor: 4.406

4. Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors: P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal: Exp Cell Res Date: 1960-09 Impact factor: 3.905

5. A familial syndrome of mental retardation in association with multiple congenital anomalies resembling the syndrome of Smith-Lemli-Opitz.

Authors: H Kenis; T W Hustinx
Journal: Maandschr Kindergeneeskd Date: 1967-05

6. Smith-Lemli-Opitz syndrome. Radiologic and postmortem findings.

Authors: R N Fine; J L Gwinn; E F Young
Journal: Am J Dis Child Date: 1968-04

Review 7. Dermatoglyphics in pediatric practice.

Authors: J R Miller; J Giroux
Journal: J Pediatr Date: 1966-08 Impact factor: 4.406

8. A syndrome characterized by mental retardation, short stature, craniofacial dysplasia, and genital anomalies occurring in siblings.

Authors: H R Blair; J K Martin
Journal: J Pediatr Date: 1966-09 Impact factor: 4.406

9. The syndrome of retardation with urogenital and skeletal anomalies in siblings.

Authors: L Dallaire; F C Fraser
Journal: J Pediatr Date: 1966-09 Impact factor: 4.406

9 in total

7 in total

1. Blocking cholesterol synthesis impairs acquisition of the classically conditioned eyeblink response.

Authors: W T O'Brien; G Xu; G S Tint; G Salen; R J Servatius
Journal: Integr Physiol Behav Sci Date: 2000 Apr-Jun

2. Smith-Lemli-Opitz syndrome: review and report of two affected siblings.

Authors: V P Johnson
Journal: Z Kinderheilkd Date: 1975

Review 3. The Smith-Lemli-Opitz syndrome.

Authors: R I Kelley; R C Hennekam
Journal: J Med Genet Date: 2000-05 Impact factor: 6.318

4. Smith-Lemli-Opitz syndrome.

Authors: S N Tomaraei; B Sarkar; A Bansali; R K Marwaha
Journal: Indian J Pediatr Date: 1993 Jan-Feb Impact factor: 1.967

5. The Smith-Lemli-Opitz syndrome. A detailed pathological study as a clue to a etiological heterogeneity.

Authors: E D Cherstvoy; G I Lazjuk; T I Ostrovskaya; I A Shved; G I Kravtzova; I W Lurie; A I Gerasimovich
Journal: Virchows Arch A Pathol Anat Histopathol Date: 1984

Review 6. Smith-Lemli-Opitz syndrome.

Authors: Andrea E DeBarber; Yasemen Eroglu; Louise S Merkens; Anuradha S Pappu; Robert D Steiner
Journal: Expert Rev Mol Med Date: 2011-07-22 Impact factor: 5.600

Review 7. Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

Authors: M L Merrer; M L Briard; S Girard; N Mulliez; C Moraine; M C Imbert
Journal: J Med Genet Date: 1988-02 Impact factor: 6.318

7 in total