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Volumn 134 A, Issue 1, 2005, Pages 100-102
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Myhre's syndrome in a girl with normal intelligence [3]
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Author keywords
[No Author keywords available]
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Indexed keywords
CLONIDINE;
GROWTH HORMONE;
ADULT;
AORTA STENOSIS;
AUTOSOMAL DOMINANT DISORDER;
BONE RADIOGRAPHY;
CARDIOGRAPHY;
CASE REPORT;
CLEFT LIP;
CONDUCTION DEAFNESS;
CONGENITAL HEART MALFORMATION;
CONGENITAL MALFORMATION;
CONSANGUINEOUS MARRIAGE;
CRYPTORCHISM;
DIFFERENTIAL DIAGNOSIS;
EYE MALFORMATION;
FACE DYSMORPHIA;
FAMILY HISTORY;
FEDERMAN MOORE SYNDROME;
FEMALE;
GENETIC DISORDER;
GOMBO SYNDROME;
GROWTH RETARDATION;
HUMAN;
INHERITANCE;
INTELLIGENCE;
JOINT MOBILITY;
KARYOTYPE;
LETTER;
LOW BIRTH WEIGHT;
MENARCHE;
MENTAL DEFICIENCY;
MENTAL DEVELOPMENT;
MOTOR DEVELOPMENT;
MUSCLE HYPERTROPHY;
MYHRE RUVALCABA SYNDROME;
PERCEPTION DEAFNESS;
PHYSICAL EXAMINATION;
PRIORITY JOURNAL;
PROVOCATION TEST;
RARE DISEASE;
SEXUAL DEVELOPMENT;
SHORT STATURE;
SKELETON MALFORMATION;
SUBTELOMERIC REARRANGEMENT;
SYNDROME DELINEATION;
TELOMERE;
VAGINAL DELIVERY;
ABNORMALITIES, MULTIPLE;
ADOLESCENT;
CHILD;
CHILD, PRESCHOOL;
CLEFT LIP;
FEMALE;
FOLLOW-UP STUDIES;
GROWTH DISORDERS;
HAND DEFORMITIES, CONGENITAL;
HEART DEFECTS, CONGENITAL;
HUMANS;
INTELLIGENCE;
SKULL;
SYNDROME;
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EID: 15744367489
PISSN: 15524825
EISSN: None
Source Type: Journal
DOI: 10.1002/ajmg.a.30444 Document Type: Letter |
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Times cited : (17)
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References (8)
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