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The Journal of Clinical Dysmorphology
|
January 1, 1983
Short broad thumbs and mental retardation in two brothers without facial dysmorphia
P Meinecke
The Journal of Pediatrics
|
June 1, 1982
Marfan-like features and congenital contractural arachnodactyly
P Meinecke
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family
P Meinecke
Clinical Genetics
|
December 1, 1986
Cryptophthalmos-syndactyly syndrome without cryptophthalmos
P Meinecke
American Journal of Medical Genetics
|
February 15, 1993
Confirmation of a particular but nonspecific metacarpophalangeal pattern profile in patients with the Smith-Magenis syndrome due to interstitial deletion of 17p
P Meinecke
American Journal of Medical Genetics
|
March 1, 1987
Evidence that the "neurofibromatosis-Noonan syndrome" is a variant of von Recklinghausen neurofibromatosis
P Meinecke
Klinische Padiatrie
|
March 1, 1982
[Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)]
P Meinecke
American Journal of Medical Genetics
|
August 1, 1990
Terminal deletion of chromosome 3p in adults: a fourth observation
P Meinecke
American Journal of Medical Genetics
|
January 1, 1987
A genetic association between microcephaly and lymphedema
P Meinecke
Journal of Medical Genetics
|
March 1, 1987
Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12q
P Meinecke, R Meinecke
Page
of 10
Search research articles
Search
Showing results (1-10 of 93) with videos related to
Sort By:
Page
of 10
The Journal of Clinical Dysmorphology
|
January 1, 1983
Short broad thumbs and mental retardation in two brothers without facial dysmorphia
P Meinecke
The Journal of Pediatrics
|
June 1, 1982
Marfan-like features and congenital contractural arachnodactyly
P Meinecke
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family
P Meinecke
Clinical Genetics
|
December 1, 1986
Cryptophthalmos-syndactyly syndrome without cryptophthalmos
P Meinecke
American Journal of Medical Genetics
|
February 15, 1993
Confirmation of a particular but nonspecific metacarpophalangeal pattern profile in patients with the Smith-Magenis syndrome due to interstitial deletion of 17p
P Meinecke
American Journal of Medical Genetics
|
March 1, 1987
Evidence that the "neurofibromatosis-Noonan syndrome" is a variant of von Recklinghausen neurofibromatosis
P Meinecke
Klinische Padiatrie
|
March 1, 1982
[Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)]
P Meinecke
American Journal of Medical Genetics
|
August 1, 1990
Terminal deletion of chromosome 3p in adults: a fourth observation
P Meinecke
American Journal of Medical Genetics
|
January 1, 1987
A genetic association between microcephaly and lymphedema
P Meinecke
Journal of Medical Genetics
|
March 1, 1987
Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12q
P Meinecke, R Meinecke
Page
of 10